Location: India (Remote)
Company: Syneos Health
Job ID: 25107322
Experience Required: 3–5 years (Not suitable for freshers)
Job Type: Talent Pipeline / Future Hiring Opportunity
About the Company
Syneos Health is a leading, fully integrated biopharmaceutical services organization that accelerates the journey from clinical development to commercialization. With operations across 100+ countries and a strong global workforce, the organization partners with pharmaceutical, biotech, and medical device companies to deliver data-driven healthcare solutions.
Role Overview
This Medical Writer role is part of a future hiring pipeline designed to identify and engage top talent for upcoming opportunities in India. Professionals selected into this talent pool will be considered for key medical writing roles supporting global clinical development programs, regulatory submissions, and scientific communications.
The position demands strong scientific writing expertise, regulatory knowledge, and the ability to translate complex clinical data into clear, compliant, and high-quality documentation.
Key Responsibilities
Lead and manage end-to-end medical writing deliverables for clinical studies with minimal supervision
Prepare, review, and finalize a wide range of regulatory and scientific documents including:
Clinical Study Protocols and Amendments
Clinical Study Reports (CSRs)
Investigator Brochures and Informed Consent Forms
Patient Narratives and Safety Reports (PSUR, DSUR)
IND, NDA, and eCTD submissions
Manuscripts, abstracts, posters, and scientific presentations
Ensure compliance with global regulatory standards such as ICH guidelines and Good Publication Practices
Coordinate cross-functional reviews with teams including Biostatistics, Data Management, Regulatory Affairs, and Medical Affairs
Perform literature searches and integrate scientific evidence into documentation
Review statistical outputs (tables, figures, listings) to ensure accuracy and consistency in reporting
Manage document quality, formatting, and editorial standards in line with AMA Manual of Style
Act as peer reviewer and mentor for junior medical writers
Support process improvements, training initiatives, and internal capability building
Required Qualifications
Master’s or Doctoral degree in Life Sciences, Pharmacy, Medicine, or related field
3–5 years of professional experience in medical writing within CRO, pharmaceutical, or medical device industry
Strong knowledge of FDA, ICH, and global regulatory guidelines
Proven experience in writing regulatory and clinical documents
Excellent command of written English, scientific communication, and document structuring
Familiarity with AMA Manual of Style and publication standards
Why This Opportunity Matters
Work on global clinical and regulatory projects across therapeutic areas
Gain exposure to high-impact regulatory submissions and scientific publications
Collaborate with international stakeholders in a fully remote setup
Be part of a strong talent pipeline for future high-growth roles in medical writing
Important Note for Applicants
This is not an immediate opening but a strategic talent pipeline role. Candidates who apply will be considered for upcoming opportunities based on business requirements.
Freshers are not eligible for this role. Entry-level candidates are advised to begin with roles such as Medical Writing Trainee, Clinical Data Associate, or Pharmacovigilance Associate to build relevant experience.
How to Apply
Interested candidates can apply via the official careers page or register through global job platforms.
For verified pharma, clinical research, and medical writing job updates, visit ThePharmaDaily.com
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Witney |Ontario :
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Oulu |Southwest Finland (Varsinais-Suomi) :
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