Senior Medical Writer (Abstracts, Manuscripts)

Syneos Health

6-10 years

Not Disclosed

Gurugram India

10 Jan. 9, 2026

Job Description

Job Type: Full Time Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Medical Writer – Abstracts & Manuscripts

Company: Syneos Health
Location: Gurugram, Haryana, India (Hybrid)
Job Type: Full-Time
Experience Required: 6–10 Years
Job ID: 25104370
Last Updated: December 24, 2025

Job Overview

Syneos Health is seeking an experienced Senior Medical Writer (Abstracts and Manuscripts) to support high-impact clinical research and publication activities. This role involves leading complex medical writing projects, mentoring junior writers, and delivering high-quality scientific documents in compliance with global regulatory and journal standards.

The position is ideal for professionals with strong expertise in clinical publications, manuscript development, abstracts, posters, and scientific communication within a CRO, pharmaceutical, or biopharmaceutical environment.

About Syneos Health

Syneos Health is a leading global biopharmaceutical solutions organization with operations in over 110 countries and a workforce of 29,000+ professionals. The company has supported 94% of FDA-approved novel drugs and 95% of EMA-authorized products in the last five years, delivering excellence across clinical development, medical affairs, and commercialization.

At Syneos Health, patient-centricity, innovation, and collaboration drive every project.

Key Responsibilities

Lead and manage medical writing activities for assigned clinical studies and publication projects with minimal supervision
Act as the primary medical writing lead and technical point of contact for internal teams and clients
Mentor and guide junior and mid-level medical writers on complex writing assignments
Develop, review, and finalize scientific documents including:
- Clinical journal manuscripts
- Conference abstracts and posters
- Scientific presentations and client deliverables
Review statistical analysis plans (SAPs), tables, figures, and listings (TFLs) for scientific accuracy, consistency, and clarity
Ensure compliance with journal guidelines, congress requirements, SOPs, client standards, and approved templates
Collaborate cross-functionally with data management, biostatistics, regulatory affairs, and medical affairs teams
Serve as a peer reviewer, providing scientific and editorial feedback on draft and final documents
Conduct online clinical literature searches and reference management
Develop high-quality scientific figures using tools such as GraphPad Prism and Adobe Illustrator
Support publication planning using software such as Datavision
Monitor project timelines, budgets, and resource utilization, escalating issues when required
Stay current with evolving regulatory guidelines and industry best practices in medical writing
Complete administrative and compliance-related tasks within defined timelines
Minimal travel may be required (less than 25%)

Required Qualifications & Experience

Master’s or PhD in Life Sciences, Pharmacy, Medicine, or a related scientific discipline
6–10 years of professional experience in medical writing, clinical publications, or regulatory documentation
Proven experience writing and leading abstracts, manuscripts, and scientific publications
Strong understanding of clinical trial design, biostatistics, and regulatory requirements
Experience working in a CRO, pharmaceutical, or biopharmaceutical organization
Excellent written English, scientific communication, and stakeholder management skills
Familiarity with global publication standards (ICMJE, GPP, CONSORT) preferred

Why Join Syneos Health

Career development and structured progression opportunities
Supportive leadership and continuous learning culture
Global exposure to high-impact clinical research projects
Inclusive and diverse work environment with a strong focus on employee well-being
Competitive compensation and total rewards program

Equal Opportunity Statement

Syneos Health is committed to creating a diverse, inclusive, and accessible workplace. The company encourages applications from candidates with transferable skills and provides reasonable accommodations in accordance with applicable laws and regulations.

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Senior Medical Writer (Abstracts, Manuscripts)

Job Description

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