Senior Medical Writer Opportunity at Syneos Health – Remote (India)

Advance your career in clinical research and scientific documentation with Syneos Health, a top global CRO. We are hiring Senior Medical Writers (CSR, IB, Protocol) to work remotely from India. Ideal candidates hold a Bachelor’s or Master’s in Life Sciences or Pharmacy and have 5+ years of experience in regulatory or clinical medical writing.

This is your chance to join a global leader trusted by 94% of FDA novel drug approvals and over 200 international clinical studies. This position offers work-from-home flexibility, competitive pay, and involvement in impactful regulatory documents.

Why Join Syneos Health?

A Trusted Name in Pharma Services

Syneos Health is a fully integrated biopharmaceutical solutions provider. We help bring therapies to market faster by combining medical, clinical, and commercial expertise. With 29,000 professionals across 110 countries, we’re reshaping how treatments reach patients.

Flexible Remote Work Model

Work remotely from anywhere in India, collaborate with global teams, and lead high-value documentation projects while enjoying work-life balance.

Continuous Development & Rewards

Technical training & domain expertise
Peer recognition programs
Diversity-driven “Total Self” workplace culture

Job Responsibilities

As a Senior Medical Writer, you will lead the development of high-quality regulatory and scientific documents:

Key Responsibilities

Prepare CSRs, clinical protocols, IBs, and IND/NDA submissions
Interpret clinical data and ensure document accuracy
Conduct literature reviews and ensure copyright compliance
Review statistical plans and outputs
Coordinate with cross-functional teams (regulatory, data, biostats)
Mentor junior writers and ensure internal quality reviews
Adhere to global guidelines like ICH E3 and AMA Style

Document Types You’ll Handle

Clinical Study Reports (CSR)
Clinical Protocols & Amendments
Investigator Brochures (IB)
Informed Consent Forms
Regulatory Submission Documents (IND, NDA, eCTD)
Scientific Publications, Abstracts, Posters

Qualifications

Educational Requirements

Bachelor’s or Master’s in Life Sciences, Pharmacy, Medicine, or related fields

Required Experience

5+ years of experience in medical writing in CRO, pharma, or device organizations
Proficient in writing regulatory and scientific documents
Strong command of English grammar and medical terminology