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Senior Medical Writer (Abstracts, Manuscripts)

Syneos Health
Syneos Health
6-10 years
Not Disclosed
10 Jan. 9, 2026
Job Description
Job Type: Full Time 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 (Remote)

Company: Syneos Health
Location: Remote – India
Job Type: Full-Time
Work Mode: Remote
Experience Required: 6–10 Years
Job ID: 25104370
Last Updated: December 24, 2025


Job Overview

Syneos Health is seeking an accomplished Senior Medical Writer (Abstracts and Manuscripts) to join its global medical writing team in a remote capacity. This role is responsible for leading high-quality scientific and clinical publication deliverables, including manuscripts, abstracts, posters, and presentations, while ensuring compliance with global regulatory, journal, and publication standards.

The ideal candidate will bring strong expertise in clinical publications, cross-functional collaboration, and mentoring junior writers, along with the ability to independently manage complex writing projects in a fast-paced, global environment.


About Syneos Health

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

The organization is built on a patient-centric Clinical Development model and a strong commitment to innovation, inclusion, and professional growth.


Key Responsibilities

  • Lead and manage medical writing deliverables for assigned clinical studies and publication projects

  • Act as the primary medical writing lead and technical contact for internal stakeholders and clients

  • Mentor and guide junior and mid-level medical writers on complex scientific writing assignments

  • Develop, write, and review high-quality scientific documents, including:

    • Clinical journal manuscripts

    • Conference abstracts and posters

    • Scientific presentations and client-facing materials

  • Review statistical analysis plans (SAPs) and tables, figures, and listings (TFLs) for scientific accuracy, clarity, and consistency

  • Collaborate with cross-functional teams including data management, biostatistics, regulatory affairs, and medical affairs

  • Serve as a peer reviewer, providing scientific and editorial feedback on draft and final documents

  • Ensure compliance with journal guidelines, congress requirements, SOPs, client standards, and approved templates

  • Conduct online clinical literature searches and reference reviews as required

  • Develop scientific figures and visualizations using tools such as GraphPad Prism and Adobe Illustrator

  • Support publication planning activities using platforms such as Datavision

  • Monitor timelines and budgets for assigned projects and communicate risks proactively

  • Stay current with evolving regulatory guidelines and industry best practices impacting medical writing

  • Complete administrative and compliance-related tasks within defined timelines

  • Minimal travel may be required (less than 25%)


Required Qualifications & Experience

  • Master’s degree 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

  • Demonstrated expertise in abstracts, manuscripts, and scientific publications

  • Strong understanding of clinical trial design, biostatistics, and publication standards

  • Prior experience in a CRO, pharmaceutical, or biopharmaceutical organization preferred

  • Familiarity with global publication and ethical guidelines (ICMJE, GPP, CONSORT)

  • Excellent written English, editing, and stakeholder communication skills

  • Ability to work independently in a remote, global team environment


Why Join Syneos Health

  • Fully remote work opportunity with global project exposure

  • Structured career development and continuous learning programs

  • Collaborative, inclusive, and employee-centric culture

  • Opportunity to contribute to high-impact clinical research and publications

  • Competitive compensation and comprehensive total rewards program


Equal Opportunity Statement

Syneos Health is an equal opportunity employer committed to fostering a diverse, inclusive, and accessible workplace. Candidates with transferable skills are encouraged to apply. Reasonable accommodations are provided in accordance with applicable laws.