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Medical Writer

U73100MH2004PTC144454 PPD Pharmaceutical Development India Private Limited

LocationIndia
SeniorityJunior to mid-level
CompanyU73100MH2004PTC144454 PPD Pharmaceutical Development India Private Limited
Verified recentlyNov 13
Compensation

Salary not listed

Salary details are shown when available from the source listing. Sign in before applying so the role can be reviewed against your resume, salary goals, seniority, timezone, and location eligibility.

Requirements and working style

Decision details from the source listing

Experience

2+ years stated

Education

Bachelor's degree in a scientific discipline or equivalent relevant formal academic or vocational qualification

Schedule

fixed

These fields are normalized from the employer's text. Confirm details on the employer site before applying.

WFH.team analysis

What this posting tells you

Full-time Medical Writer role in India. The writer authors routine clinical documents, summarizes study data, supports regulatory writing, and collaborates with project teams. The listing specifies a standard Monday–Friday schedule and approximately 2+ years of relevant experience. It labels the role fully remote but also describes an office work environment.

Role lane

Administrative and data entry, Data, Education, Healthcare admin, Operations, Product, Security, Writing and content

Where you can work

India

Working hours

Asia/Kolkata

Arrangement

Junior to mid-level · full_time

Required signals
Medical and scientific writingClinical study report and study protocol writingData interpretation and presentationRegulatory documentation knowledgeEditing and proofreadingCommunicationOrganization and planningAttention to detail
Preferred signals
Pharmaceutical or CRO industry experienceScientific writing experienceExperience with document management systemsExcel and Outlook
Confirm before applying
  • Compensation is not listed
Market context

Administrative and data entry hiring on WFH.team

1,113active related roles
335new in the latest period
36.3jobs per 100 candidates
$165kmedian of comparable listed ranges

Category counts come from WFH.team's latest published remote job market snapshot.

Explore the remote job market
Skills and signals
Medical and scientific writingClinical study report and study protocol writingData interpretation and presentationRegulatory documentation knowledgeEditing and proofreadingCommunicationOrganization and planningAttention to detailPharmaceutical or CRO industry experienceScientific writing experienceExperience with document management systemsExcel and OutlookListed as fully remote in India, but the description also says work is performed in an office environment.
Job description

Medical Writer at U73100MH2004PTC144454 PPD Pharmaceutical Development India Private Limited

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Medical Writer - Make an Impact at the Forefront of Innovation

The Medical Writer provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients. The role involves collaborating with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence.

What you'll do

  • Serve as primary author who writes and provides input on routine documents such as clinical study reports and study protocols, and summarizes data from clinical studies.
  • May assist with more complex clinical and scientific and program level documents, including IBs, INDs, and MAAs.
  • Ensure compliance with quality processes and requirements for assigned documents. May assist in determining best practices, methods and techniques for achieving optimal results.
  • May assist in program management activities. Duties could include assisting with developing timelines, budgets, and forecasts for assigned deliverables.
  • Represent the department at project launch meetings, review meetings, and project team meetings.

Education & Experience Requirements

  • Bachelor's degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification
  • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years).
  • Experience working in the pharmaceutical/CRO industry preferred
  • Experience in scientific writing advantageous

Years of experience refers to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions.

Knowledge, Skills, Abilities

  • Solid medical writing skills, including grammatical, editorial, and proofreading skills
  • Ability to interpret and present complex data accurately and concisely
  • Effective administrative, organizational and planning skills; attention to detail and quality
  • Ability to work on own initiative and effectively within a team
  • Effective oral and written communication skills
  • Good knowledge of regulatory documentation and drug development process
  • Great judgment and decision-making skills
  • Good computer skills and skilled with client templates; Good knowledge of document management systems and other relevant applications (e.g. Excel, Outlook)

Working Conditions and Environment

  • Work is performed in an office environment.
  • Exposure to electrical office equipment.
  • Occasional drives to site locations with occasional travel both domestic and international.
  • Long, varied hours required occasionally.

Why Join Us?

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthroughs.