Introduction

Medical writing course assists you to indite content related to healthcare, science and covers all forms of medical journalism to medical education. Moreover, it also helps you to write about the medical marketing of healthcare products. The most important part is, the medical writing course also focuses on the publication and presentation of research documents and regulatory documents. 

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A trained medical writer is well-versed with scientific and health terms and concepts. Furthermore, they perceive prowess to translate all clinical, scientific data and information efficiently into various formats for different target audiences.

Medical writing courses are a top trend nowadays, and it is expanding because of the needs of the health industry. 

Medical writers are enthusiastically engaged by pharmaceutical companies, research organizations, communications agencies, regulatory agencies, scientific journals, and medical websites. In addition, they know how to prepare varieties of documents that are required for regulatory submissions in a drug or medical device development.

This course will also help you comprehend medical device development processes such as clinical trial level documents- protocols, study reports, annual safety updates, etc. Medical writing is a short-duration professional course that covers all indispensable segments of medical writing. Medical writing certification is recognized by the industry.

Henry Harvin has come up with the latest seven modules in medical writing to hone your skills and get the adept solutions of healthcare.

 

  • Foundation Module: It includes the acquisition of knowledge about the basics of medical writing, guidelines required for medical writing, the scope of medical writing, valuable important features, planning, layout, and core elements of medical writing.
  • Scientific Writing Style: It alludes to scientific news, scientific reviews, scientific research papers for journals, and case reports.You can expedite your scientific writing styles by using different methods.
  • Drug Development Process: It helps you to comprehend the drug development process- from pre-clinical development to clinical development, research to clinical study designs to post-marketing scrutinization.
  • Clinical/ Non-clinical Writing: Candidates will acquire knowledge of the distinction between Clinical and Non- Clinical Writing about the international Conference on Harmonisation Guidelines, Good Laboratory Practices, and recapitulation of Non-Clinical content and study reports.
  • Medical Writing for Clinical Trials: Learners will learn to unravel medicinal product dossiers and can get expertise in writing about this segment. In addition, you will be able to write brochures, protocol, Development safety update reports, and many more.
  • Medical Writing in Post Marketing Phase: This module will guide you in writing aggregate reports, Risk management, clinical study reports, etc.
  • Instructions and guidelines to publish Clinical Data: You can explore more in Consolidated criteria for Reporting Qualitative research, Advocacy , Restoration, and Educational, Technology Recreation Education Nature and Discovery, etc.
  •  Henry Harvin provides 16 hours of Live Online interactive classroom services to enrich your knowledge. Fees for medical writing courses are affordable not merely for affluent families but others also. So the total emoluments for this course are Rs. 12,500.

Job 6

Company Name : makro

Designation: Medical Associate

Location: telangana

Experience: 2 – 5 years

Qualification :

  • UG :Any Graduate in Any Specialization
  • PG :Post Graduation Not Required

Job Description :

  • Prepare and provide functional / Clinical area inputs in preparation of clinical documents (Protocols, Studies, Study reports), Labeling, and other clinical study reports for both Drugs and medical devices
  • Aid in preparation of documents & responses to health authorities in addition to documents such as clinical overviews and summaries, etc.
  • Be accountable for quality and adherence to timelines at different stages of all projects
  • Perform detailed literature search utilizing both public and private databases and show apt while synthesizing the results
  • Coordinate with other cross functional teams in the data review, analysis and reporting of clinical studies.
  • Be responsible as Author and sometimes in conjunction with another medical writer, for overall content and accuracy of study report before forwarding for final signoff.
  • Assist with internal and external dissemination of results to the Development Team, Investigators etc.
  • Provide mentoring, and training for other team members
  • Work with multinational project teams and coordinate activities on multiple projects Function independently with initiative and minimal guidance
  • Have attention to detail and focus on quality
  • Work effectively in a team setting, take over additional responsibilities
  • Travel to client locations involved for some projects as needed.
  • Other responsibilities as assigned by company

Post Graduate Program in Medical Writing

Henry Harvin® Medical Writing Course Ranks #1 online by Higher Education Digest | Strengthen your writing prowess as you boost your skills as a Medical and Scientific Writer

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Salary : Not Disclosed

Website:http://jobs.makrogrp.com/Jobdetails.aspx?job_id=10178&state=Telangana&job_state=&keyword=&category=&lbl=Medical+Associate&job_category=29&source=Makro-Care

Email Id: www.makrocare.com

Job 5

Company Name : TNQ Technologies Pvt Ltd

Designation: Medical Writer – Freelancer

Location: Chennai

Experience: 3 – 8 years

Qualification :

  • PG :Any Postgraduate in Any Specialization
  • Doctorate :Any Doctorate in Any Specialization

Job Description :

  • Audio MP3 files; Writers doc with authors information
  • Supplemental materials: These materials include important points referred to in the program, with special attention paid to accuracy of medical and pharmacological terminology
  • Summary of the audio file to be transcribed into content complying to stipulated number of words and pages
  • Compliance to the style guide, style manual and other requisites as mentioned in the tutorial video are warranted
  • Prepare a list of related journal references for each program, drawing from Medline, in-house texts and journals, and syllabus material accompanying the lectures
  • Develop educational objectives for each program, adhering to the guidelines as specified
  • Prepare 10 multiple-choice questions for each program based on the educational objectives of the program
  • Read and review pertinent scientific literature to remain current on topics in given medical specialty

Salary : Not Disclosed

Address: Plot No. 4/600 4/197,,PHASE II,DR. VIKRAM SARABHAI, INSTRONIC ESTATE,,KOTTIVAKKAM, THIRUVANMIYUR, , Chennai, Tamilnadu, India

Job 4

Company Name : Tevapharm India Private Ltd 

Designation: Medical writer-Bangalore

Location: Bangalore/Bengaluru

Experience: 5 – 7 years

Qualification :

  • UG :B.Pharma in Pharmacy, Any Graduate in Any Specialization
  • PG :M.Pharma in Any Specialization

Job Description :

  • Prepare CSR, appendices and other relevant documents (Swiss medic checklist, bio summary tables, module 2.7, CS-BE etc.) as per the regulatory/sponsor requirements in the required format.
  • Coordinate with all concerned departments to ensure timelines and compliance to regulatory/sponsor requirements for preparation, compilation and delivery of reports.
  • Preparation of study reports for CE/PK studies, Brand studies
  • Attend medical writing related sponsor queries.
  • Prepare amended reports and amendments to the CSR when necessary.
  • Electronically generate, review study documents and submission of study reports in CTD/eCTD format as per regulatory requirements.
  • Providing coding for all adverse events recorded in the study as per MedDRA coding system for clinical trials.
  • Attend medical writing related sponsor queries.
  • Quality check of the final compiled study reports for delivery.
  • Responsible for providing practical training to new recruits regarding the preparation of CSR, appendices and other relevant documents.
  • Report to Lead Medical Writing-Reports.
  • To carry out other responsibilities as and when assigned by management.

Salary : Not Disclosed

Contact Number : 91-22-2570-5681

Job 3

Company Name : Yashoda Super Speciality Hospital

Designation: Walkin – Medical Content Writer -Yashoda Corporate Office

Location: Hyderabad/Secunderabad

Experience: 4 – 8 years

Qualification : 

  • UG :Any Graduate in Any Specialization
  • PG :Any Postgraduate in Any Specialization

Job Description :

  • Medical Content: Should have experience and be adept at medical content writing. Medical and clinical knowledge is a must. Writing, Editing, and proofreading medical content. Writing should be comprehensive while ensuring technical information i.e. medical content should become easy for the masses (social media audience) to understand.
  • Copywriting: Write, edit & review original copies/content for marketing assets such as Social media, SEM Ads, email campaigns, notifications, SMS, and other consumer-facing touch-points.
  • Collaborate with the Design & Product team to develop marketing material.
  • Establish social media presence and manage Yashoda Groups social platforms
  • To monitor competition activities, trends within the Medical Management & Hospital fraternity.
  • Internal & External stakeholder relations: Content Agencies, Doctors, HODs & relevant Internal teams.
  • Stay updated on medical and consumer information in the medical field, especially current trends.

Salary : Not Disclosed

Contact Number : +91 40 4567 4567

Job 2

Company Name : Siro Clinpharm Pvt. Ltd.

Designation: Medical Writer – MBBS/ MD Fresher

Location: Mumbai, Hyderabad/Secunderabad

Experience: 0 – 2 years

Qualification : 

  • UG :MBBS in Any Specialization
  • PG :Medical-MS/MD in Any Specialization

Job Description :

  • Will be responsible for conceptualizing and drafting clinical development documents like CSRs, IB, Protocols, Narratives, Concept notes etc. with adequate oversight and in compliance with documented guidelines, SOPs, and timelines
  • Performing scientific and medical review of all regulatory documents to make them scientifically sound and medically logical
  • Applying medical knowledge for developing study concepts and drug development plans.
  • Co-ordinate and discuss with investigators, sites and internal operations teams for robust medical writing documents.
  • Interact with statisticians, programmers and data managers for a well-integrated document
  • Review and contribute to drug safety related documentation
  • Support new and existing business
  • Support senior management by providing business decks and dashboards on a regular periodic basis.

Salary : Not Disclosed

Address: UNIT NO 3 and 4,IST FLOOR,KALPATARU PRIME,ROAD NO , 16,WAGLE INDUSTRIAL ESTATE THANE W, , THANE, Maharashtra, India

Job 1

Company Name : INCNUT DIGITAL PRIVATE LIMITED

Designation: Freelance Content Writer/Medical writer

Location: Kolkata, Mumbai, Hyderabad/Secunderabad, Pune, Chennai, Bangalore/Bengaluru, Delhi / NCR

Experience:2 – 7 years

Qualification :

  • UG :Graduation Not Required, Any Graduate in Any Specialization
  • PG :Any Postgraduate in Any Specialization, Post Graduation Not Required
  • Doctorate :Doctorate Not Required, Any Doctorate in Any Specialization

Job Description :

Able to meet weekly targets/ work consistently

Salary :Not Disclosed

Contact Person :IncNut Digital Pvt Ltd

G-3 (Ground Floor),Modern Profound Tech Park,Whitefields, Kondapur,Hyderabad – 500081, Telangana

Website :https://www.incnut.com/

     6/4/2021

Company Name : WebMD

Designation: WebMD : Medical Writer / Reviewer

Location: Navi Mumbai

Experience: 3 – 8 years

Qualification : 

  • UG :MBBS in Medicine
  • PG :Medical-MS/MD in Any Specialization, MDS in Any Specialization
  • Doctorate :Other Doctorate, Any Doctorate in Any Specialization

Job Description :

  • To write clinical summaries/news for a physician audience, bringing them the latest updates from various sources like clinical research publications/professional medical practice/regulatory authority/medical conferences/medical information
  • Should be familiar with use of databases like Pubmed, Ovid, Medical conference sites
  • Responsible for all content-related aspects of each assigned project from initiation to launch, including conception, writing, revising, annotating per source references, and performing QA checks.
  • Copy must be accurate, clean, well-organized, and adhere to WebMD technical specifications.
  • Project and Workload Management: Must be able to handle multiple projects concurrently, maintain highest quality, and meet copy deadlines.
  • Must be able to interact effectively with internal teams (i.e., editorial, and production) to ensure quality and smooth progression of projects.
  • Curating content in proprietary format

Salary : Not Disclosed

Website: http://www.webmd.com

Job 9

Company Name : EVERSANA INDIA PRIVATE LIMITED

Designation: Medical Writer

Location: Hyderabad/Secunderabad, Pune, Bangalore/Bengaluru, Mumbai

Experience: 2 – 7 years

Qualification :

UG :B.Pharma in Any Specialization, BDS in Any Specialization

PG :MDS in Any Specialization, M.Pharma in Any Specialization

Job Description :

  • Serves as medical writer for several brands; depending on experience level, may also act as lead medical writer and reviewer on his/her own brand(s)
  • Ensures correct grammar, spelling, and usage, as well as adherence to AMA, agency, and client styles
  • Ensures accuracy of data and claims by thoroughly fact checking references; and resolving fact-checking issues
  • Demonstrates a passion for clarity, an eye for detail, and be able to address issues of word flow, logic, and layout
  • Ensures brand-specific style is consistent throughout jobs; maintains and updates assigned client style guides
  • Works closely with team members to ensure materials are of the highest quality in terms of accuracy, utility, clarity, readability and appeal
  • Participates in weekly status meetings for assigned accounts; works with supervisor to assess resource needs
  • Acts as a resource for internal teams relative to AMA style and brand consistency
  • Assists with tagging and linking of pieces to be submitted to clients Medical-Legal-Regulatory review committee on Veeva Vault, as needed
  • Flag possible compliance issues as they arise
  • Keep current on industry practices and regulatory requirements that affect medical content and copy

All other duties as assigned

Salary : Not Disclosed

Address: G/101-103,1ST Floor,SR. N.o 15/1 To 15/6, MARISOFT, -I,Vadgaon Sheri,PUNE, , PUNE, Maharashtra, India

Website: http://www.eversana.com

Job 8

Company Name : InVentiv International Pharma Services Pvt. Ltd

Designation: SENIOR MEDICAL WRITER – CSR & PROTOCOL

Location: Hyderabad/Secunderabad, Pune, Chennai, Ahmedabad, Gurgaon/Gurugram, Delhi / NCR, Bangalore/Bengaluru, Mumbai (All Areas)

Experience: 5 to 9 year(s)

Qualification : UG:Any Graduate in Any Specialization

Job Description :

  • Mentors and leads less experienced medical writers on complex projects, as necessary.
  • Acts as lead for assigned writing projects.
  • Manages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal supervision.
  • Develops or supports a variety of documents  that include, but not  limited to:
  • Clinical study protocols and clinical protocol amendments;
  • Clinical study reports;
  • Patient narratives;
  • Clinical development plans;
  • IND submissions and annual reports;
  • Integrated summary reports;
  • NDA and (e)CTD submissions;
  • Investigator brochures, as well as;
  • Clinical journal manuscripts, clinical journal abstracts, and client presentations.
  • Identifies and proposes solutions to resolve issues and questions arising during the writing process, including resolution or escalation as appropriate.
  • Reviews statistical analysis plans and table/figure/listing specifications for appropriate content, and for grammar, format, and consistency.
  • Interacts with department head and staff members in data management, biostatistics, regulatory affairs, and medical affairs as necessary to produce writing deliverables.
  • Serves as peer reviewer on internal review team providing review comments on draft and final documents.
  • Adheres to established regulatory standards, including but not limited to ICH-E3 guidelines, as well as Company Standard Operating Procedures, client standards, and Company and/or client approved templates when completing medical writing projects, on-time and on-budget.
  • Performs on-line clinical literature searches, as applicable.
  • Maintains familiarity with current industry practices and regulatory requirements and guidelines that affect medical writing.
  • Maintains awareness of budget specifications for assigned projects, working within the budgeted hours and communicating changes to medical writing leadership.
  • Completes required administrated tasks within the specified timeframes.
  • Performs other work-related duties as assigned.

Salary : Not Disclosed by Recruiter

Address: UNIT NO. 301, 3RD FLOOR OF BLDG. NO.12B,SURVEY NO., 64 PART,MINDSPACE CYBERABAD PROJECT,MADHAPUR,MADHA, PUR, Hyderabad, Telangana, India

Job 7

Company Name : MIMS MEDICA INDIA PRIVATE LIMITED 

Designation: Urgent Requirement For Principal Medical Writer

Location: Hyderabad/Secunderabad, Bangalore/Bengaluru, Delhi / NCR, Mumbai (All Areas)

Experience: 8 – 13 years

Qualification :

  • PG :MS/M.Sc(Science) in Any Specialization, M.Pharma in Any Specialization, Medical-MS/MD in Any Specialization
  • Doctorate :Ph.D in Any Specialization

Job Description : 

  • Maintain a deep scientific understanding of clients’ and competitors brand portfolios in order to proactively provide tailored and insightful consultancy on strategic MedComms solutions
  • Use scientific knowledge to produce a full spectrum of MedComms content, including manuscripts/publications, symposium highlights, newsletters, detail aids, slide decks, digital content, etc
  • Provide leadership to key account team(s) to assure scientific accuracy, strategic alignment with the relevant client communications programs, and high-quality output that helps to build the scientific foundation for client brands
  • Maintain knowledge of, and relationships with, key opinion leaders in key therapeutic areas in order to provide guidance and recommendations to clients
  • Lead and facilitate discussions amongst key opinion leaders during briefings, speaker reviews, ad boards and manuscript development, to ensure the successful delivery of events and other medical communications projects
  • Lead the delivery of the scientific and editorial components of onsite events
  • Cultivate strong relationships with clients commercial and medical contacts through credibility demonstrated by medical communication knowledge and interpersonal consultancy skills
  • Proactively seek new business opportunities
  • Lead client meetings/teleconferences for project kick-off and delivery and strategic planning
  • In collaboration with Client Services and Business Managers ensure continued growth of key accounts and securing of new business through industry leading pitches and proposal development
  • Provide line management to Medical Writer(s), setting clear goals and expectations, career and development plans and monitoring and evaluating performance
  • Provide training, coaching and mentoring of editorial and other colleagues on scientific and therapy area knowledge, compliance and editorial standards

Salary : Not Disclosed

Address: 02,,Margosa Building,13th Cross Margosa Road,Malle, swaram, , BANGALORE, Karnataka, India

Job 6

Company Name : Siro Clinpharm Pvt. Ltd.

Designation: Medical Writer – MBBS/ MD Fresher

Location: Mumbai, Hyderabad/Secunderabad

Experience: 0 – 2 years

Qualification :

  • UG :MBBS in Any Specialization
  • PG :Medical-MS/MD in Any Specialization

Job Description :

  • Will be responsible for conceptualizing and drafting clinical development documents like CSRs, IB, Protocols, Narratives, Concept notes etc. with adequate oversight and in compliance with documented guidelines, SOPs, and timelines
  • Performing scientific and medical review of all regulatory documents to make them scientifically sound and medically logical
  • Applying medical knowledge for developing study concepts and drug development plans.
  • Co-ordinate and discuss with investigators, sites and internal operations teams for robust medical writing documents.
  • Interact with statisticians, programmers and data managers for a well-integrated document
  • Review and contribute to drug safety related documentation
  • Support new and existing business
  • Support senior management by providing business decks and dashboards on a regular periodic basis.

Salary : Not Disclosed

Address: UNIT NO 3 and 4,IST FLOOR,KALPATARU PRIME,ROAD NO , 16,WAGLE INDUSTRIAL ESTATE THANE W, , THANE, Maharashtra, India

Job 5

Company Name : Biocon Limited

Designation: Clinical Development Lead

Location: Bangalore/Bengaluru

Experience: 5 – 10 years

Qualification : PG :Medical-MS/MD in Any Specialization

Job Description :

  • Prepares/Reviews CDP, IB, study protocols, ICF, scientific advice, TLF’s, and CSRs.
  • Attends standing meetings of boards, committees, etc. as and when required.
  • Provides/Reviews medical inputs for study conduct as per applicable GCP, SOP, and regulatory requirements.
  • Provides inputs on study-level data including GCP-issues report.
  • Attends regular meetings with CRO and/or other vendors.
  • Supports and oversees activities of study conduct e.g. site selection, interaction with investigators, and other service providers.
  • Accountable for the accuracy of trial information in all trial Registries such as Clinical Trials Registry – India (CTRI), Clinicaltrials.gov, etc.
  • Contributes to medical aspects and takes part in study initiation and investigator meetings.
  • Provides/Reviews inputs into protocol deviation decision.
  • Oversees CRO and conducts study-specific medical monitoring which includes a review of daily lab alerts and SAEs to communicate with CRO regarding follow-up.
  • Supports audits and inspections.
  • Supports budget preparation of clinical trials (if required).
  • Monitors safety of subjects participating in clinical trials.
  • Supports the pharmacovigilance department in preparing safety documents.
  • Supports the statistics team in the conduct of Data Safety Monitoring Board interim analysis meetings.
  • Supports in DBL (provide inputs on Tables, Listings, and Figures, participate in all DBL meetings).
  • Prepares/Reviews CDPs, Protocol Synopsis/Protocol, IB, ICF, Safety forms, etc.
  • Reviews study documents e.g. SAP, DMP, SMP, DSMB charter, MMP, Imaging charter.
  • Provides inputs on final TLFs, works with the medical writer to review & revise CSR documents, draft discussion and conclusions, participate in comment resolution meetings.
  • Leads Regulatory and MAA approvals (USFDA/EMA/PMDA/CDSCO and other regulatory authorities across different regions and countries) for clinical aspects.
  • Interacts with CAB/ Advisory committees/DSMB members.
  • Supports in Handling of Regulatory, Marketing or any other molecule-related queries
  • Medical monitoring which includes data reviews, EDC reviews.
  • Prepares/Reviews IND / IMPD medical documents, annual updates, MAA/CTD, and other regulatory submission medical documents.
  • Supports department activities like SOP preparation and review / external potential partner scientific discussions/consultant interaction.
  • Supports the dissemination of important scientific information through articles or presentations or training
  • Performs other related duties as assigned

Salary : Not Disclosed

Address: BIOCON LTD,HOSUR ROAD,20TH KM,ELECTRONIC CITY,BANG, ALORE, , BANGALORE, Karnataka, India

Contact Number : +91 80 2808 2808

Email Id: [email protected]

Job 4

Company Name : Cytel Statistical Software & Services Pvt. Ltd.

Designation: Senior Value Communications Writer

Location: India

Experience: 2 – 5 years

Qualification :

  • UG :Any Graduate in Any Specialization
  • PG :Post Graduation Not Required

Job Description : 

  • Writing fully-referenced content, for global value dossiers, country submissions, scientific manuscripts, slide decks, and related deliverables, based on clinical, scientific, and pharmacoeconomic evidence
  • Developing simple visuals and graphics (e.g., in Excel or PowerPoint) Editing, fact-checking, and formatting Acting as a lead writer on project teams
  • Daily communication and teamwork with colleagues in the Value Communications team and with subject matter experts in other Cytel/PSE groups
  • Project management tasks such as developing timelines and drafting meeting minutes, and conducting routine email and phone communication with clients
  • Workload management to meet internal and client-driven deadlines

Salary : Not Disclosed

Contact Number : +(617) 661-2011

Email Id: [email protected]

Website:https://careers.cytel.com/job/Senior-Value-Communications-Writer/727721500/

Job 3

Company Name : SwitchLane Inc.

Designation: Medical Case Writer & Researcher

Location:Chennai 

Experience:5 – 10 years

Qualification :

PG :MS/M.Sc(Science) in Biochemistry, Biology, Medical-MS/MD in Biochemistry, Immunology, Microbiology

Job Description :

  • Deal candidates have a Master’s Degree or higher in biochemistry, chemistry, molecular biology, physiology, immunology, neuroscience or other similar science fields. Any related experience in the medical field is a plus.
  • Candidates should be disciplined, organized, have strong writing skills and fast internet suitable for remote work.
  • Willing to work in the US Shift hours
  • Position duties include review of patients’ past medical record histories to summarize pertinent findings for the physician, preparing the chart for the patient visit following a predetermined diagnostic and treatment flow, recording patient data subsets appropriately, and research projects for specific topics and conditions as assigned.
  • Required strong written communication skills

Salary :Not Disclosed

Address:10/17 ANANDAM COLONY,,,SOUTH CANAL BANK ROAD,MANDA, VELLI, , Chennai, Tamilnadu, India

Contact Number :+91-044-48534316

Job 2

Company Name :WebMD

Designation:Medical Writer / Reviewer 

Location:Navi Mumbai

Experience:3 – 8 years

Qualification :

  • UG :MBBS in Medicine
  • PG :Medical-MS/MD in Any Specialization, MDS in Any Specialization
  • Doctorate :Other Doctorate, Any Doctorate in Any Specialization

Job Description :

  • To write clinical summaries/news for a physician audience, bringing them the latest updates from various sources like clinical research publications/professional medical practice/regulatory authority/medical conferences/medical information
  • Should be familiar with use of databases like Pubmed, Ovid, Medical conference sites
  • Responsible for all content-related aspects of each assigned project from initiation to launch, including conception, writing, revising, annotating per source references, and performing QA checks.
  • Copy must be accurate, clean, well-organized, and adhere to WebMD technical specifications.
  • Project and Workload Management: Must be able to handle multiple projects concurrently, maintain highest quality, and meet copy deadlines.
  • Must be able to interact effectively with internal teams (i.e., editorial, and production) to ensure quality and smooth progression of projects.
  • Curating content in proprietary format

Salary :Not Disclosed

Website:http://www.webmd.com

Job 1

Company Name :EVERSANA INDIA PRIVATE LIMITED

Designation:Medical Writer

Location: Hyderabad/Secunderabad, Pune, Bangalore/Bengaluru, Mumbai (All Areas)

Experience:2 – 7 years

Qualification :

  • UG :B.Pharma in Any Specialization, BDS in Any Specialization
  • PG :MDS in Any Specialization, M.Pharma in Any Specialization

Job Description :

  • Serves as medical writer for several brands; depending on experience level, may also act as lead medical writer and reviewer on his/her own brand(s)
  • Ensures correct grammar, spelling, and usage, as well as adherence to AMA, agency, and client styles
  • Ensures accuracy of data and claims by thoroughly fact checking references; and resolving fact-checking issues
  • Demonstrates a passion for clarity, an eye for detail, and be able to address issues of word flow, logic, and layout
  • Ensures brand-specific style is consistent throughout jobs; maintains and updates assigned client style guides
  • Works closely with team members to ensure materials are of the highest quality in terms of accuracy, utility, clarity, readability and appeal
  • Participates in weekly status meetings for assigned accounts; works with supervisor to assess resource needs
  • Acts as a resource for internal teams relative to AMA style and brand consistency
  • Assists with tagging and linking of pieces to be submitted to clients Medical-Legal-Regulatory review committee on Veeva Vault, as needed
  • Flag possible compliance issues as they arise
  • Keep current on industry practices and regulatory requirements that affect medical content and copy
  • All other duties as assigned

Salary :Not Disclosed

Address:G/101-103,1ST Floor,SR. N.o 15/1 To 15/6, MARISOFT, -I,Vadgaon Sheri,PUNE, , PUNE, Maharashtra, India

Contact Number : Marisoft IT Park, Tower – 1, 101 – 103, 1st Floor, Kalyani Nagar, Pune, Maharashtra 411014

30/3/2021

Job 5 :

Company Name : MIMS MEDICA INDIA PRIVATE LIMITED 

Designation: Principal Medical Writer

Location: Mumbai

Experience: 8 – 13 years

Qualification :

  • PG :MS/M.Sc(Science) in Any Specialization, M.Pharma in Any Specialization, Medical-MS/MD in Any Specialization
  • Doctorate :Ph.D in Any Specialization

Job Description :

  • Maintain a deep scientific understanding of clients’ and competitors brand portfolios in order to proactively provide tailored and insightful consultancy on strategic MedComms solutions
  • Use scientific knowledge to produce a full spectrum of MedComms content, including manuscripts/publications, symposium highlights, newsletters, detail aids, slide decks, digital content, etc
  • Provide leadership to key account team(s) to assure scientific accuracy, strategic alignment with the relevant client communications programs, and high-quality output that helps to build the scientific foundation for client brands
  • Maintain knowledge of, and relationships with, key opinion leaders in key therapeutic areas in order to provide guidance and recommendations to clients
  • Lead and facilitate discussions amongst key opinion leaders during briefings, speaker reviews, ad boards and manuscript development, to ensure the successful delivery of events and other medical communications projects
  • Lead the delivery of the scientific and editorial components of onsite events
  • Cultivate strong relationships with clients commercial and medical contacts through credibility demonstrated by medical communication knowledge and interpersonal consultancy skills
  • Proactively seek new business opportunities
  • Lead client meetings/teleconferences for project kick-off and delivery and strategic planning
  • In collaboration with Client Services and Business Managers ensure continued growth of key accounts and securing of new business through industry leading pitches and proposal development
  • Provide line management to Medical Writer(s), setting clear goals and expectations, career and development plans and monitoring and evaluating performance
  • Provide training, coaching and mentoring of editorial and other colleagues on scientific and therapy area knowledge, compliance and editorial standards

Salary : Not Disclosed

Contact : 022 6612 2600

Job 4 :

Company Name : IQVIA RDS India Pvt Ltd 

Designation: Medical Writer

Location: Cochin, Mumbai, Bengaluru

Experience: 5 – 9 years

Qualification :

  • UG :B.Pharma in Any Specialization
  • PG :M.Pharma in Any Specialization

Job Description :

  • Manage day-to-day workload: identify project needs, track timelines and implement customer requests, keeping manager/senior staff abreast of progress on tasks and any potential problems with project work.
  • Lead customer meetings independently.
  • May give a presentation to an existing customer (e.g. to discuss templates, results, lessons learned), responding appropriately to feedback.
  • May deliver basic level training to small groups or individuals within IQVIA on the role of the medical writer, on medical writing processes, or on specific customer templates/processes. May also provide guidance to more junior colleagues.
  • May take the role of Project Manager for a small and short Medical Writing project.
  • Complete project finance activities, including monitoring and forecasting budgeted hours.
  • Understand budgets and project finance principles. Interact with Project Leader/Project Finance Manager directly regarding straightforward financial issues, increasing ability to estimate hours needed for more straightforward/routine tasks. ;
  • May propose revisions to standard operating procedures (SOPs) or suggest process improvements for consideration.

Salary : Not Disclosed

Website: https://jobs.iqvia.com/

Job 3 :

Company Name : CACTUS

Designation: Medical Editor

Location: Secunderabad, Pune, Bengaluru

Experience: 0 to 5 year

Qualification :

  • PG:MS/M.Sc(Science) in Any Specialization,M.Pharma in Any Specialization,MDS in Any Specialization,Medical-MS/MD in Any Specialization
  • Doctorate:M.Phil. in Dermatology,Any Doctorate in Any Specialization,Ph.D in Any Specialization

Job Description :

  • Edit different document types for global pharmaceutical clients, including but not limited to checks on language and grammar, technical terminology, and accuracy of data
  • Format documents based on journal/congress guidelines
  • Ensure that the document adheres to specified style guides
  • Consistently deliver a high-quality edit, exceeding client expectations every time
  • Contribute to team initiatives like knowledge sharing exercises and documentation of resources

Salary : Not Disclosed

Email Id: [email protected]

Job 2:

Company Name : SUNDYOTA NUMANDIS PHARMACEUTICALS PRIVATE LIMITED

Designation: Scientific & Medical Affairs

Location: Ahmedabad

Experience: 0 – 2 years

Qualification :

  • UG :B.Pharma in Any Specialization
  • PG :M.Pharma in Any Specialization

Job Description :

  • Conduct biomedical literature search
  • Provide evidence based medical & scientific information
  • Timely production of high quality documents manuscript, abstracts, review articles, research articles, case reports, scientific reports

Salary : Not Disclosed

Contact : +91 79 48916511 +91 79 48916512/13/14/15

Email Id: [email protected]

Job 1 :

Company Name : Kelly Outsourcing and Consulting Group India

Designation: Global Medical Advisor

Location: Bengaluru

Experience:

  • UG :MBBS in Any Specialization
  • PG :Medical-MS/MD in Any Specialization, MDS in Any Specialization

Job Description :

  • Interest in product/ clinical trial details
  • Strong attention to details
  • Interpreting and communicating Scientific Data (Scientific Communication)
  • Flair for research, medical writing
  • Expected to be a medical expert of the specific product

Salary :₹ 9,50,000 – 18,00,000 P.A.

Contact: 080670 81800

17/3/2021

Job:4

Company Name: The Himalayan Drug

Designation: Scientific Manager (Medical Writing & Medical Affairs)

Location: Bangalore/Bengaluru

Experience: 1 – 5 years

Qualification: UG :MBBS in Any Specialization

PG :Medical-MS/MD in Any Specialization

Job Description: 

Roles and Responsibilities

  • Responsible for preparation & review of clinical trial documents (Investigators Brochure, Protocol, ICD) and interpretation of clinical data and other complex information in a most acceptable quality document (Interim Report or Clinical Study Report)
  • Act as liaison between Scientific affairs team and Clinical Operations study team to provide highest quality clinical trial documents.
  • Review and provide the scientific feedback on the essential documents related to conduct of clinical trial.
  • Write and review scientific abstracts, publication, related to clinical studies. Provide scientific inputs on healthcare website, health magazine etc. Work closely with multidisciplinary group of experts to translate the study data and results into presentations, reports, regulatory documents, scientific journal manuscripts and abstracts for publication.
  • Should conduct comprehensive literature searches to enhance background understanding and evaluate and analyze the information.
  • Regular interaction with KOL in various therapeutic area and discussing on various factors for marketing, product positiong strategy
  • Interacting with the potential investigators prior to the protocol writing on the design, startegy and feasibility of conducting the study
  • Support in medical affairs activities related to Himalaya products. Provide support to marketing team for responding scientifically to the medical queries raised by the Doctors/ Field staff.

Skills Requirement:

  • Data interpretation and medical writing skills, including grammatical, editorial, and proofreading skills. Good knowledge of English grammar with a familiarity of writing clinical trial documents
  • Knowledge of global, regional, national and other document development guidelines
  • Comfort of searching the scientific matter available on open resources.
  • Ability to communicate scientific or medical information in a clear and concise manner
  • Should possess good training skills to conduct trainings at various platforms
  • In order to be effective in job, a Scientific Manager must be aware of current industry practices and regulatory requirements. Must keep abreast of current literature, emerging science, technological developments and medical trends.

Desired Candidate Profile

  • Degree in modern medicine (MBBS/MD). Fresher or with 2-3 years of relevant experience of medical writing and scientific strategy (related to Clinical Trials Document & Publications) at sponsor or CRO Company.
  • Hands on experience in literature search, targeted literature review, preparation of scientific document, disease or drug related literature on the basis of data available from publications.
  • Experience in preparation of clinical trial documents, scientific abstracts, publication would be preferred
  • Thorough knowledge of clinical trial concepts, including ICH-GCP, CFR and regulatory guidelines (DCGI, USFDA, MHRA)

Role Documentation/Medical Writing

Industry Type Medical, Healthcare, Hospitals

Functional Area Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology

Employment Type Full Time, Permanent

Role Category Drug Regulatory Affairs/Documentation

Salary: Not Disclosed

Address: THE HIMALAYA DRUG COMPANY,,THE HIMALAYA DRUG COMPA, NY,TUMKUR ROAD,MAKALI,

Job:3

Company Name: inVentiv International Pharma Services Pvt. Ltd.

Designation: SENIOR MEDICAL WRITER – CSR & PROTOCOL

Location: Hyderabad/Secunderabad, Pune, Ahmedabad, Gurgaon/Gurugram, Chennai, Bangalore/Bengaluru, Delhi / NCR, Mumbai (All Areas)

Experience: from 5 to 9 year(s) of Experience

Qualification: UG:Any Graduate in Any Specialization

Job Description: 

Roles and Responsibilities

Serves as a senior medical writer on clinical study or regulatory project teams. Writes, edits, and coordinates content for clinical/regulatory while serving as primary technical contact with the internal team and the client.

JOB RESPONSIBILITIES

  • Mentors and leads less experienced medical writers on complex projects, as necessary.
  • Acts as lead for assigned writing projects.
  • Manages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal supervision.
  • Develops or supports a variety of documents  that include, but not  limited to:
  • Clinical study protocols and clinical protocol amendments;
  • Clinical study reports;
  • Patient narratives;
  • Clinical development plans;
  • IND submissions and annual reports;
  • Integrated summary reports;
  • NDA and (e)CTD submissions;
  • Investigator brochures, as well as;
  • Clinical journal manuscripts, clinical journal abstracts, and client presentations.
  • Identifies and proposes solutions to resolve issues and questions arising during the writing process, including resolution or escalation as appropriate.
  • Reviews statistical analysis plans and table/figure/listing specifications for appropriate content, and for grammar, format, and consistency.
  • Interacts with department head and staff members in data management, biostatistics, regulatory affairs, and medical affairs as necessary to produce writing deliverables.
  • Serves as peer reviewer on internal review team providing review comments on draft and final documents.
  • Adheres to established regulatory standards, including but not limited to ICH-E3 guidelines, as well as Company Standard Operating Procedures, client standards, and Company and/or client approved templates when completing medical writing projects, on-time and on-budget.
  • Performs on-line clinical literature searches, as applicable.
  • Maintains familiarity with current industry practices and regulatory requirements and guidelines that affect medical writing.
  • Maintains awareness of budget specifications for assigned projects, working within the budgeted hours and communicating changes to medical writing leadership.
  • Completes required administrated tasks within the specified timeframes.
  • Performs other work-related duties as assigned.

Desired Candidate Profile

  • Minimum 5 Years of experience in Regulatory Medical Writer Role
  • Should have Authored P II – III CSR or Protocol documents
  • Should have worked on ICF or IB Documents
  • Should have experience in Leading the Project or Client

Role: Clinical Research Associate/Scientist

Salary: Not Disclosed by Recruiter

Industry: Pharma, Biotech, Clinical Research

Functional Area: Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology

Role Category: R&D

Employment Type: Full Time, Permanent

Salary: Not Disclosed by Recruiter

Address: UNIT NO. 301, 3RD FLOOR OF BLDG. NO.12B,SURVEY NO., 64 PART,MINDSPACE CYBERABAD PROJECT,MADHAPUR,MADHA, PUR, Hyderabad, Telangana, India 

Job:2

Company Name: Celegence Systems Private Limited

Designation: Medical Writer (CER Specialist) – Medical Device

Location: Bangalore/Bengaluru( Bannerghatta Road )

Experience: 1 – 5 years

Qualification: UG :B.U.M.S in Any Specialization, MBBS in Any Specialization, B.Pharma in Any Specialization, BAMS in Any Specialization, BHMS in Any Specialization, Other Graduate, B.Sc in Any Specialization

Job Description:

Roles & Responsibilities:

  • Ensure on-time development and delivery of high-quality CERs compliant with MEDDEV 2.7/1 Rev. 4. And EU MDR for devices across therapeutic areas
  • Be adept at delivering solutions that are customized per the client requirements
  • Assist in the development of schedules to ensure client CER timelines are met
  • Perform literature searches, screen and summarize literature for relevant clinical evidence
  • Study device-specific client documents and report device characteristics and instructions for use
  • Summarize data from post-marketing surveillance and perform risk analysis for the devices in scope
  • Actively engage with cross-functional client business teams such as Medical Directors, Post Market Surveillance, Design Quality Engineers, R&D, and Regulatory Affairs relating to the CER process
  • Work with the team and Team Lead to prepare documents that meet client expectations in terms of content, format, and presentation
  • Manage timelines and communicate with team members to maintain awareness of expectations, milestones, and deliverables
  • Conduct proofreading, editing, document formatting, review comment integration and document completion / approval activities.

Desired Candidate Profile

  • Bachelors Degree / Post Graduation in any relevant Life Sciences fields. Masters Degree is preferred.
  • RAC certification is a plus
  • Minimum 2 years of relevant CER experience required
  • Familiar with the Life Sciences Industry, preferably Regulatory Services
  • Hands on experience on CER to perform their job role.
  • Experience in creating customer facing materials
  • Ability to work independently
  • Fluent in English

Technical / Functional Skills:

  • Experience within the medical device industry and knowledge of clinical evaluation report, regulatory requirements, evidence generation, and CER document creation
  • Experience in Literature Search, Review and Analysis, Risk Benefit Assessment, Equivalency Approach, Post Market Surveillance Data Analysis including Trend CER Analysis, Non-Clinical/Clinical Data (pre-clinical, Sponsored studies/IIR), State of the Art (SotA) and Conclusions.
  • Experience in performing medical literature searches (PubMed, Google Scholar, etc.)
  • Hands on experience on presentation tools like PowerPoint, Visio etc. will be an added advantage.

Role Documentation/Medical Writing

Industry Type Pharma, Biotech, Clinical Research

Functional Area Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology

Employment Type Full Time, Permanent

Role Category Drug Regulatory Affairs/Documentation

Salary: Not Disclosed

Address: 175,176,,91 SPRINGBOARD,BANNERGHATTA ROAD JP NAGAR, 4TH PHASE,BENGALURU, , BANGALORE, Karnataka, India

Job:1

Company Name: 1mg

Designation: Hiring For Medical Content Writer @1mg || Gurgaon

Location: Gurgaon/Gurugram

Experience: 1 – 6 years

Qualification: UG :Any Graduate in Any Specialization

Job Description:

Looking for a Medical Content Writer who has experience in writing high-quality, value-based content. 

Must-haves:

-Research a topic to find unique insights that provide readers with new, useful information and advice.

-Empathy for healthcare seekers and curiosity to understand their needs and wants.

-Communicate complex topics in ways that are relatable and understandable for the target audience.

-Ancillary support for day-to-day activities of different verticals owned by Medical affairs     

-Medical/Pharma/Biotech/Microbiology as Educational background

Good-to-have

-Versed with SEO Sops

Role content Writer

Industry Type Medical, Healthcare, Hospitals

Functional Area Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology

Employment Type Full Time, Permanent

Role Category Not mentioned

Salary: ₹ 3,50,000 – 6,00,000 P.A.

Address: 1MG TECHNOLOGIES PRIVATE LIMITED Tower -B-46/4, 5th floor, Presidency Building, Mehrauli, Gurgaon Sector 14

9/3/2021

Job: 10

Company Name: ALS MEDICAL EDUCATION PVT LTD

Designation: Medical safety Writer

Location: Chandigarh, Lucknow, Ranchi

Experience: 0 – 5 years

Qualification: UG :MBBS in Any Specialization

Job Description: 

Medical Content Writer required for rephrasing content for MBBS and MD/MS Students.

Freelance / Remote job. Payment Rs.300 for every 600 words rephrased. Only candidates with MBBS Degree and strong English should apply.

Role Medical Officer

Industry Type Medical, Healthcare, Hospitals

Functional Area Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology

Employment Type Part Time, Freelance/Homebased

Role Category Medical Professional

Salary: ₹ 50,000 – 60,000 P.A.

Address B204, PLOT 36, SECTOR 4, DWARKA, DELHI

Job: 9

Company Name: TNQ Technologies Pvt Ltd

Designation: Medical Writing Associate

Location: Chennai

Experience: 3 – 8 years

Qualification: PG :Any Postgraduate in Any Specialization

Doctorate :Any Doctorate in Any Specialization

Job Description: 

Roles and Responsibilities

Interpret audio files on different genres of medicine and transcribe to written format

Input:

1. Audio MP3 files; Writers doc with authors information

2. Supplemental materials: These materials include important points referred to in the program, with special attention paid to accuracy of medical and pharmacological terminology

Required Output:

3. Summary of the audio file to be transcribed into content complying to stipulated number of words and pages

4. Compliance to the style guide, style manual and other requisites as mentioned in the tutorial video are warranted

5. Prepare a list of related journal references for each program, drawing from Medline, in-house texts and journals, and syllabus material accompanying the lectures

6. Develop educational objectives for each program, adhering to the guidelines as specified

7. Prepare 10 multiple-choice questions for each program based on the educational objectives of the program

8. Read and review pertinent scientific literature to remain current on topics in given medical specialty

Salary: Not Disclosed

Address Plot No. 4/600 4/197,,PHASE II,DR. VIKRAM SARABHAI, INSTRONIC ESTATE,,KOTTIVAKKAM, THIRUVANMIYUR, , Chennai, Tamilnadu, India

Job: 8

Company Name: Acubel IT Solutions

Hiring for Potentiam Offshore Services

Designation: Medical Affairs Medical Writing

Location: Hyderabad/Secunderabad, Chennai, Bangalore/Bengaluru

Experience: 6 – 10 years

Qualification: UG :B.Tech/B.E. in Biomedical

PG :M.Tech in Biomedical

Job Description: 

We seek a highly skilled Principal Medical Writers /Team Lead Medical Writers.

The Principal Medical writer should have the skills and ambition to work as a Team lead.

Ownership and responsibility for his/her teams development and delivery of scientifically

accurate content that is aligned with client objectives and meets the specification, budgetary and

schedule requirements

Management of his/her line report(s), demonstrating leadership and direction to achieve efficient

and profitable delivery of work through effective resourcing; ensuring individuals are provided

with opportunities to grow and develop their role within the agency

Duties & Responsibilities:

Technical

  • Strategic communication programmes and complex projects development and

implementation; ability to write scientific, technical and strategic medical/marketing

documents

  • Apply therapy and marketing knowledge to pitch and proposal development and delivery
  • Scientific strategy and facilitation for client meetings; excellent KOL knowledge and

management

Managerial

  • Performance management (objective setting, appraisal), leadership, motivation of team
  • Leadership and direction to ensure timely delivery of quality content
  • Recruitment, training and staff development
  • Implementation of NexGen SOPs, act as role model

Financial

  • Partnering with the AD on accounts to deliver revenue targets and ensure work is

Salary: ₹ 10,00,000 – 20,00,000 P.A.

Address Koramangala, Bangalore

Job: 7

Company Name: Siro Clinpharm Pvt. Ltd.

Designation: Medical Writer – Medico Marketing

Location: Thane

Experience: 0 – 2 years

Qualification: UG :MBBS in Any Specialization

PG :Medical-MS/MD in Any Specialization

Job Description: 

  • Will be trained on Authoring all regulatory documents including CSRs, IB Updates, Protocols (including conceptualization), and Narratives in compliance with documented guidelines, SOPs, and timelines
  • Draft medical writing deliverables in accordance with documented guidelines, SOPs and timelines and .
  • Will further be performing scientific and medical review of all regulatory documents including CSRs, IB Updates, Protocols, and Narratives.
  • Applying medical knowledge for developing study concepts and drug development plans.
  • Support new and existing business.
  • Support senior management by providing business decks and dashboards on a regular periodic basis for management meetings.

Salary: Not Disclosed

Websitehttps: //www.siroclinpharm.com/

Address UNIT NO 3 and 4,IST FLOOR,KALPATARU PRIME,ROAD NO , 16,WAGLE INDUSTRIAL ESTATE THANE W, , THANE, Maharashtra, India

Job: 6

Company Name: Parexel International India Pvt. Ltd.

Designation: Medical Writing – MBBS/MD

Location: 

Mohali, Mumbai, Chandigarh, Hyderabad/Secunderabad, Pune, Ahmedabad, Delhi / NCR, Bangalore/Bengaluru

Experience: from 2 to 7 year(s) of Experience

Qualification: UG:B.Sc in Any Specialization,BDS in Any Specialization,B.Pharma in Any Specialization,BAMS in Any Specialization

Job Description: 

Experience in Aggregate reporting is a must.

Preparing end to end PSURs (including ad-hoc requests) in accordance with client requirements/conventions and Standard Operating Procedures (SOPs)

• Liaising with the relevant stakeholders regarding discrepancies, and for obtaining incomplete/missing information (where required), in order to resolve and clarify issues and to facilitate processing of the reports

• Maintaining excellent knowledge of the safety profile of the assigned products, clients procedures and international drug safety regulations

• Maintaining an awareness of global regulatory requirements and reporting obligations and organizing workload to ensure compliance with timelines communicated by the client

• Performing self QC of reports

• Ensuring MedRDA coding in accordance with MedRDA Term Selection: points to consider where applicable

Salary: Not Disclosed by Recruiter

Contact Company: Parexel International India Pvt. Ltd.

Address: Building No.20,11th Floor,Sundew Properties Ltd SE, Z,Raheja Mindspace,HItech city, Madhapur, , Hyderabad, Telangana, India

Job: 5

Company Name: Medvarsity Online Limited

Designation: Medical Writing-Bio technology

Location: Hyderabad/Secunderabad

Experience: 1 – 5 years

Qualification: UG :MBBS in Any Specialization

Job Description: 

About this Job:

The Medical Writer is responsible for ensuring high-quality medical review and editing (quality assessments) during the development and delivery of e-learning modules for various medical courses.

The deliverables include E-learning modules, course handbooks, presentations, medical animations, educational videos, interactive case studies, etc.

The role is part of a team of content developers and reports to the content development manager.

Responsibilities:

  • Perform medical review and quality edits for various course materials.
  • Coordinate with and manage a community of subject matter experts, freelance medical writers, and other content contributors.
  • Ensure that the quality requirements, authoring standards and delivery deadlines are met for course materials.
  • Provide any support to authors during the E-learning development cycle.
  • Coordinate with other team members such as instructional designers, animators,
  • video editors to ensure that the content has a high user engagement and learning impact.
  • Drive continuous improvement initiatives for improving efficiencies and improving overall content quality.
  • Plan your time effectively and work with senior team members to ensure you can meet deadlines on multiple projects.
  • Some project and client management as agreed with senior team members.
  • Other activities prescribed by the content development manager.

Salary: ₹ 50,000 – 60,000 P.A.

Address Life Sciences Building,2nd Floor,,Apollo Hospital , Complex,Jubilee Hills, , Hyderabad, Telangana, India

Job: 4

Company Name: Yogam BPO Hiring for Yogam Bpo

Designation:Medical Writing Assistant

Location: Kolkata, Mumbai, Hyderabad/Secunderabad, Pune, Chennai, Bangalore/Bengaluru

Experience: 0 – 5 years

Qualification: UG :B.El.Ed in Any Specialization, B.P.Ed in Any Specialization, B.B.A / B.M.S in Management, B.Com in Commerce, Other Graduate

Job Description: 

Inviting Medical Graduates for a Career in Medical Scribe.

Night shift.

Online Certification provided.

Along with training as a Medical Scribe role you require general medical terminology, strong typing and documentation skills

Salary: Not Disclosed

Website http://www.yogambpo.org

Address YOGAM BPO ONLINE TRAINING ACADEMY PROVIDES SKILL BASED JOB SESSIONS IN MEDICAL TRANSCRIPTION, MEDICAL CODING CPC, MEDICAL SCRIBING, MEDICAL WRITING, MEDICAL BILLING, CLINICAL RESEARCH / PV / CDM / meDRA CODING. Whats-App 9789004777 / Call 9840040143

Job: 3

Company Name: GlaxoSmithKline Pharmaceuticals Limited

Designation: Associate Medical Writer Digital Health

Location: 

Bangalore/Bengaluru

Experience: from 6 to 10 year(s) of Experience

Qualification: UG:Any Graduate in Any Specialization

PG:M.Pharma in Pharmacy,MS/M.Sc(Science) in Microbiology

Doctorate:Doctorate Not Required

Job Description: 

Contributes to documents and activities to be included in registration files.

Authors clinical documents following defined templates.

Ensures the consistency and quality level of all documents that are issued.

Actively participates in all planning, coordination and review meetings.

Ability to work on 2-3 assignments simultaneously.

Proactively raises and discusses concerns/ issues in an open and timely manner and within the global team at GSK Vaccines, thereby demonstrating the ability of promoting high scientific standards by pointing out obvious flaws and proposing (and advocates) alternatives.

Works directly with diversity of roles at different levels within GSK (e.g., Clinical Research and Development Leader (CRDL), Project Level CRDL, Regional Medical Directors and Advisors, Study Delivery Leads (SDL), Study Data Managers (SDM), Biostatisticians, other Scientific Writers).

Establishes network of communication and continuously builds collaboration to facilitate smooth partnerships and interfaces between all groups involved in delivery of writing assignments.

Salary: Not Disclosed by Recruiter

Contact Company: GlaxoSmithKline Pharmaceuticals Limited

Job: 2

Company Name: Supportmart Technical Services Pvt. Ltd.

Designation: Scientific Writer

Location: Gurgaon/Gurugram

Experience: 3 – 8 years

Qualification: UG :Any Graduate in Any Specialization

PG :Any Postgraduate in Any Specialization

Job Description: 

Job purpose:

Full-time Content Editor is responsible for creating, editing and/or acquiring content for

websites, email newsletters and other online communications media such as podcasts, etc.

Key responsibilities and accountability:

The nature of online content

Online content can take many forms, including plain text, links, database content, still images

(illustrations, photographs, diagrams), animation, audio, video, interactive devices (forms,

forums, chat rooms, polls, questionnaires, etc.). The main responsibility of the editor will be for

the creation or acquisition of verbal content (primarily textual but also audio), although a close

relationship with other media specialists, such as graphic designers, will almost certainly be

required.

Work elements

• Design and development: The editor is unlikely to be primarily responsible for design

and development. They will, however, contribute an important user-orientated

perspective to the process. Contribute to audience research as a basis for design of the

site. Contribute to the top-level and detailed design of the website (or e-newsletter,

etc.), with a particular focus on the ways in which the goals for the site and the needs of

users can be met through the provision of appropriate content. Contribute to the

process of information design, to ensure that content is appropriately structured to

meet the goals for the site and the needs of users. Contribute to documentation of the

design. Contribute to the selection or design of appropriate content management

software.

Salary: ₹ 3,00,000 – 5,00,000 P.A.

Address 30,UDYOG VIHAR PHASE 1,,,SECTOR-20,GURGAON, , , GURGAON, Haryana, India  

Job: 1

Company Name: POPULAR MEDICARE LIMITED

Designation: Sr. Medical Writer/ Medical Writer

Location: Varanasi/Benaras

Experience: 2 – 5 years

Qualification: PG :Any Postgraduate in Any Specialization

Job Description: 

*Writing clear marketing copy to promote our services

*Preparing well-structured drafts using Content Management Systems

*Coordinate with marketing and design teams to illustrate articles

*Update website as needed

*Promote content on social media

Role Documentation/Medical Writing

Industry TypeMedical, Healthcare, Hospitals

Functional AreaMedical, Healthcare, R&D, Pharmaceuticals, Biotechnology

Employment TypeFull Time, Permanent

Role CategoryDrug Regulatory Affairs/Documentation

Salary: Not Disclosed

Address DLW Road, Opposite Flyover, Kakkarmatta, Varanasi Contact No. 9519999324  

3/3/2021

Job: 10

Company Name: Parexel International India Pvt. Ltd.

Designation: Manager Medical Writing

Location:  

Mohali, Mumbai, Chandigarh, Hyderabad/Secunderabad, Pune, Ahmedabad, Delhi / NCR, Bangalore/Bengaluru

Experience: from 2 to 7 year(s) of Experience

Qualification: UG:B.Sc,BAMS,BDS,B.Pharma

Job Description: 

Experience in Aggregate reporting is a must.

Preparing end to end PSURs (including ad-hoc requests) in accordance with client requirements/conventions and Standard Operating Procedures (SOPs)

• Liaising with the relevant stakeholders regarding discrepancies, and for obtaining incomplete/missing information (where required), in order to resolve and clarify issues and to facilitate processing of the reports

• Maintaining excellent knowledge of the safety profile of the assigned products, clients procedures and international drug safety regulations

• Maintaining an awareness of global regulatory requirements and reporting obligations and organizing workload to ensure compliance with timelines communicated by the client

• Performing self QC of reports

• Ensuring MedRDA coding in accordance with MedRDA Term Selection: points to consider where applicable

Salary: Not Disclosed by Recruiter

Contact Company:Parexel International India Pvt. Ltd.

Address:Building No.20,11th Floor,Sundew Properties Ltd SE, Z,Raheja Mindspace,HItech city, Madhapur, , Hyderabad, Telangana, India

Job: 9

Company Name: Sun Pharmaceutical Industries Ltd

Designation: Senior Medical Writer

Location: 

Gurgaon/Gurugram

Experience: from 0 to 2 year(s) of Experience

Qualification: UG:MBBS

Job Description: 

Roles and Responsibilities

– Prescribing information

– Summary of Product Characteristics

– Patient Information Leaflet / Medication Guide

– Clinical Expert Reports

– Nonclinical Expert Reports

– Medical data package

– Medical Rationale/ Therapeutic justifications

– Pediatric study plans for US FDA

– Annual Report for US NDA

– Bio-recommendation and bio-waiver

– Integrated summary of safety/ efficacy

– Medical/Scientific write-up for safety and efficacy of drug products

– Scientific literature search for identification of new products

– Regulatory Writing*

Desired Candidate Profile

Salary: Not Disclosed by Recruiter

Contact Company:Sun Pharmaceutical Industries Ltd

Address:201 B/1,,SUN HOUSE,WESTERN EXPRESS HIGHWAY,GOREGAO, N EAST, , MUMBAI, Maharashtra, India

Job: 8

Company Name: BioQuest Solutions Private Limited

Designation: Team Lead Medical Writers

Location: Bangalore/Bengaluru

Experience: 3 – 7 years

Qualification: UG :BVSC, BAMS, MBBS, Other Graduate, B.Pharma

PG :Other, Medical-MS/MD, MDS, M.Pharma, MS/M.Sc(Science)

Job Description: 

Roles and Responsibilities

Job Description

  • Author (To write manuscripts, abstracts, slides, slide notes, posters)
  • Review and edit (already written manuscripts),
  • Rewrite (where required)
  • Guide (team members)
  • Preparing publication-ready documents
  • Scoping (to comprehend nature of work, the extent of involvement, set course and timelines)
  • Client interactions scientific support as a knowledge expert (to drive scientific discussions and facilitate projects)
  • Adhere to global processes, scientific code of conduct (reference backed writing) and ethics of writing (no plagiarism)
  • Adhere to project specific requirements and timelines
  • Self-upgradation continuous enhancement and upgradation of skills aligned to strategic direction
  • Handle and manage multiple tasks/ project/s independently
  • Ph.D/ PDF (at least 5-6 years into medical writing)
  • Strong research background with molecular level understanding
  • Good publication record Original research publications in international journals: peer-reviewed, high-impact would add value
  • Good knowledge of clinical trials/RWE studies
  • Good understanding of protocol and CSR elements:
  • Study design & Methodologies: laboratory/preclinical/clinical
  • Data visualization and qualitative and quantitative analysis: statistical considerations
  • Understanding of ICH/CFR/ICMJE /GPP Guidelines and checklists (CONSORT/TREND/STROBE)
  • Basic understanding of trial regulations
  • Ability to read and interpret CSRs, Narratives
  • Ability to write, proof-read, edit, review, rewrite, data synthesis
  • Conduct in-depth Literature review using PubMed, Medline, clinicaltrials.gov, EMBASE, etc.

Salary: ₹ 8,00,000 – 18,00,000 P.A.

Contact PersonJessina

Job: 7

Company Name: Inspiration Manpower Consultancy Pvt. Ltd.

Designation: Medical Content Writer

Location: Noida

Experience: 1 – 6 years

Qualification: UG :Any Graduate

Job Description: 

Job description

Interview & Work Location- Noida

Qualification – Medical education background- BDS BPT, BHMS, BAMS

Skill- Medical Underwriting

Experience- 1-8 Years in Medical Summarization or Medical Underwriting experience

Group life insurance– Mandate

Good communication skills, US Shifts, Work from Office

Can hire medical freshers for Senior Process Associate position

Only Immediate Joiners who can reallocate to Noida

Salary: ₹ 3,50,000 – 7,50,000 P.A.

Address Noida Sector -35

Job: 6

Company Name: Silmed Scientific Pvt Ltd

Designation: Senior Regulatory Medical Writer

Location: Kochi/Cochin, Bangalore/Bengaluru

Experience: 2 – 6 years

Qualification: UG :MBBS, B.Pharma

PG :M.Pharma, Medical-MS/MD, MS/M.Sc(Science)

Job Description: 

Roles and Responsibilities

We are hiring an experienced medical writer with experience in CTD medical writing and experience in clinical development of medicines.

  • Writing high quality CTD modules nonclinical and clinical overviews & summaries (Module 2.5, 2.4, 2.7, 2.7) as per requirements in EU submission
  • Response to clinical deficiencies
  • Assist with drug development strategy
  • SmPC, Patient information leaflet
  • Clinical study reports, Study design and synopsis
  • Assist in clinical development strategy Review of Study reports published papers
  • Literature search and regulatory evaluation
  • Rx to OTC evaluation
  • PSURs, PADER, RMP

Ideal candidate should have

  • Must have 3-5 years previous experience authoring global clinical submissions including, but not limited to, clinical study reports (CSRs), study protocols, informed consent forms (ICFs), protocol amendments, ICF amendments, eCTD modules specifically 2.4 – 2.7), DSURS, PBRERs and signal evaluation reports. Working knowledge of industry guidelines and standards (FDA, EMA, ICH, PMDA)
  • Scientific accuracy
  • Attention to details
  • Understanding of Generic, Hybrid and New drug applications
  • Experience in Clinical study design and protocol
  • Excellent communication skills and time management
  • Experience in Clinical and non-clinical overviews is a must

Salary: Not Disclosed

Websitehttp: //www.silmedscientific.com

[email protected],[email protected]

Job: 5

Company Name: WebMD

Designation: Medical Affairs Medical Writing

Location: Navi Mumbai

Experience: 3 – 8 years

Qualification: UG :MBBS

PG :MDS, Medical-MS/MD

Job Description: 

Education: PhD/MD/MBBS/PharmD

Experience : 5+ years

Role & Responsibility:

  • To write clinical summaries/news for a physician audience, bringing them the latest updates from various sources like clinical research publications/professional medical practice/regulatory authority/medical conferences/medical information
  • Should be familiar with use of databases like Pubmed, Ovid, Medical conference sites
  • Responsible for all content-related aspects of each assigned project from initiation to launch, including conception, writing, revising, annotating per source references, and performing QA checks.
  • Copy must be accurate, clean, well-organized, and adhere to WebMD technical specifications.
  • Project and Workload Management: Must be able to handle multiple projects concurrently, maintain highest quality, and meet copy deadlines.
  • Must be able to interact effectively with internal teams (i.e., editorial, and production) to ensure quality and smooth progression of projects.
  • Curating content in proprietary format

Primary Skills and Critical Competencies:

  • Experience with pharmaceutical/medical writing experience, or an equivalent combination of related education and experience. Experience writing for the digital environment preferred.
  • Ability to analyse complex data and interpret it for mobile/web application while maintaining a clinical tone
  • Excellent interpersonal and communications skills, both oral and written
  • Independent and innovative self-starter
  • Strong organizational skills
  • Meticulous attention to detail
  • Ability to quickly distil complex information into essential elements relevant to clinicians at the point of care
  • Excellent medical literature retrieval and evaluation skills
  • Ability to manage multiple projects in a fast-paced setting
  • Proficient knowledge of MS Word, Excel, PowerPoint
  • Basic understanding of various handheld technologies

Salary: Not Disclosed

Websitehttp: //www.webmd.com

Job: 4

Company Name:Regrow Biosciences Private Limited 

Designation: Lead – Medical Writer

Location: Mumbai

Experience: 4 – 6 years

Qualification: PG :M.Pharma, MS/M.Sc(Science)

Job Description: 

  • Review of available data and preparation of manuscript writing for publication, research paper, review paper, conference presentation, abstract, poster, book chapter and review article etc
  • Preparation of write-ups on patient case reports and product benefits for various online & offline publishing
  • Writing research proposal, clinical research report, case report & case study and clinical patient narratives
  • Prepare PPTs for conference presentations
  • Content development for various offline & online media, Blogs, website, newsletters, collaterals & PR
  • Literature research as per the need of the field force, brand development & regulatory requirement
  • Regulatory Support to clinical research team in protocol writing , communication with various regulatory authorities and accreditation bodies
  • Review and editorial support for all types of content
  • Carry out any other job-related activities as and when deemed necessary.

Salary: ₹ 3,25,000 – 3,50,000 P.A.

Address: 2ABC,2ND FLOOR,ACME PLAZA,ANDHERI KURLA ROAD,ANDHE, RI-EAST, , MUMBAI, Maharashtra, India

Job: 3

Company Name: Ozone Pharmaceuticals ltd

Designation: Regulatory Medical Writer

Location: Delhi / NCR

Experience: 3 – 5 years

Qualification: UG :MBBS, B.Pharma, B.Sc, BDS, BAMS

PG :Any Postgraduate

Job Description: 

Roles and Responsibilities

  • Conducting in-depth research on industry-related topics in order to develop original content.
  • Development of content for various drugs, diseases, and Prepares scientific documents of the highest quality meeting all applicable regulatory requirements.
  • Creating marketing and advertising pieces promoting our diagnostic or therapeutic products.
  • Developing medical professional centric content in form of blogs, articles, newsletter, social media, and the company website
  • Partners with creative services to develop highly visual and engaging materials that maintain a high level of scientific accuracy and achieve our clients strategic objectives
  • Creating various documents needed to develop educational activities for physicians and other healthcare professionals. These documents include needs assessments, slide sets, and outcomes analyses
  • Coordinate the efforts of cross-functional teams to produce high-quality, medically accurate documents and ensure consistency between related documents
  • Takes a proactive solutions-oriented approach to all tasks
  • Creating an array of materials for lay audiences, including patient education, decision aids, public health communication, website content, medical/health news, news releases, and public relations/communications.
  • Will be responsible for writing medically proclaimed content and assisting the overall content strategy based on our specific goals and objectives for Ozone Pharma.
  • To ideate campaigns with the team, turn ideas into scientific Impressions, and execute them.
  • Build a strong online value proposition for Ozone Pharma as an umbrella brand with a focus on Rx products.
  • Drive Creativity First narrative and approach towards the work

Salary: Not Disclosed

Address: A-3,,1 L.S.C,JANAK PURI,NEW DELHI, , , NEW DELHI, Delhi, India

Job: 2

Company Name: PRA Health Sciences

Designation:-Medical Underwriting | US Medical Writing

Location: India

Experience: 2 – 6 years

Qualification: UG :Any Graduate

PG :Medical-MS/MD

Job Description: 

Position overview:

Working as part of a global and wellconnected team, our Medical Writers are second-to-none. Assigned to early-phase projects, your work will be varied and fast-paced and you will benefit from the satisfaction of working on the full project lifecycle for a variety of therapeutic areas.

No two days are the same in our Medical Writing team, but typical responsibilities will include:

  • To research, write and edit clinical documents by applying functional expertise and your clinical drug development knowledge
  • To lead project teams in drafting individual report specifications and in coordinating data analysis
  • To contribute to clinical protocol development, collaborating with different functional areas from around the world
  • To consult with and advise other Medical Writers and clients in the development of clinical plan outlines

You will be encouraged to leverage your experience and benefit from the knowledge of other team members, all the time being supported by a transparent management structure designed to enable you to succeed.

PRA is the ideal place to foster your Medical Writing career. As you gain experience in PRA, there may be options to progress in to lead or functional management roles.

Qualifications

You are:

An experienced and motivated Medical Writing professional committed to making things happen.

Here at PRA we want our employees to succeed and ensure that they are set up for this success through constant training, development and support. To enable success in this position you will have:

  • A relevant educational background, preferably PhD, MD or PharmD
  • Extensive experience in medical writing
  • Robust knowledge of clinical study report writing and protocol writing
  • Ideally, you will also have previous experience working in a CRO environment, and ideally with early-phase drug development
  • Fluent English language skills
  • The ability to work well under pressure and collaborate with global team members

Salary: Not Disclosed

Website : https://careers-prahs.icims.com/jobs/61241/jobdetails/job

Job: 1

Company Name: Hindco Recruitment Consultants

Designation: Lead – Medical Writer

Location: Mumbai, Mumbai Suburban, Thane, Ghaziabad, Navi Mumbai, Hyderabad/Secunderabad, Pune, Delhi / NCR, Bangalore/Bengaluru

Experience: 0 – 5 years

Qualification: UG :Any Graduate, B.Pharma

PG :M.Pharma, Any Postgraduate

Job Description: 

– To author Medical Communications deliverables independently as per quality standards (internal external) & within expected timelines.

– It includes manuscripts, slide sets, abstracts, posters, medical education materials, systematic reviews, etc.

Required Candidate profile

– Advanced degree in life sciences/ pharmacy/ similar discipline or medical degree.

– Relevant training experience in health economics or other relevant health-related scientific discipline.

Perks and benefits

WFH, Work from Home option is available.

Salary: Not Disclosed

Address : Email: [email protected] | Upload your resume on www.jobringer.com

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31 Comments

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  15. Vijay kumar Reply

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  21. Raj molthra Reply

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  31. Amit Yadav Reply

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