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Senior Medical Writer (Abstracts, Manuscripts)

Syneos Health
Syneos Health
5-8 years
preferred by company
10 Jan. 8, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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)
Location: India – Remote
Job ID: 25104370
Industry: Medical Writing | Clinical Research | Scientific Publications
Employment Type: Full-time
Experience Required: 5–8 Years
Updated On: December 24, 2025


Job Overview

Syneos Health®, a global leader in integrated biopharmaceutical solutions, is hiring a Senior Medical Writer (Abstracts & Manuscripts) for a fully remote role in India. This position is ideal for experienced medical writers with strong expertise in scientific publications, including peer-reviewed manuscripts, congress abstracts, posters, and clinical presentations.

The role involves leading publication-focused medical writing projects, mentoring junior writers, and collaborating cross-functionally to deliver high-quality, compliant scientific content aligned with global regulatory and publication standards.


Key Responsibilities

Medical Writing & Project Leadership

  • Act as the lead medical writer for abstracts, manuscripts, posters, and scientific presentations.

  • Mentor and guide junior medical writers on complex publication deliverables.

  • Manage end-to-end medical writing activities for assigned studies with minimal supervision.

Content Development & Review

  • Write, edit, and review clinical journal manuscripts, congress abstracts, posters, and client-facing scientific presentations.

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

  • Identify, assess, and resolve issues arising during the writing process, escalating when required.

  • Serve as a peer reviewer, providing high-quality review feedback on draft and final documents.

Cross-Functional Collaboration

  • Collaborate with Biostatistics, Data Management, Regulatory Affairs, Medical Affairs, and Clinical teams to ensure accurate and timely deliverables.

  • Act as the primary scientific and technical contact for internal stakeholders and clients on assigned projects.

Compliance & Publication Standards

  • Ensure compliance with journal and congress guidelines, ICMJE/GPP standards, company SOPs, client requirements, and approved templates.

  • Maintain up-to-date knowledge of industry best practices, publication ethics, and regulatory requirements impacting medical writing.

Literature & Visualization Support

  • Conduct online clinical literature searches to support scientific content development.

  • Develop or review scientific figures and graphics using tools such as GraphPad Prism and Adobe Illustrator.

  • Utilize publication planning and tracking systems such as Datavision.

Project & Administrative Management

  • Manage project timelines and budgeted hours, proactively communicating risks or changes to leadership.

  • Complete administrative and compliance-related tasks within defined timelines.

  • Perform additional duties as assigned. Minimal travel may be required (less than 25%).


Required Qualifications

Education

  • Advanced degree preferred (PhD, MD, PharmD, MSc, or equivalent) in Life Sciences, Pharmacy, Medicine, or a related scientific discipline.

Experience

  • 5–8 years of proven experience in medical writing with a strong focus on abstracts, manuscripts, and scientific publications.

  • Demonstrated experience leading publication deliverables for clinical studies in a remote or global environment.

Technical & Professional Skills

  • Strong understanding of clinical research, data interpretation, and biostatistics concepts.

  • Proficiency in scientific writing, editing, and document coordination.

  • Experience with figure creation, data visualization, and publication planning tools.

  • Excellent written and verbal communication skills with strong attention to detail.

Core Competencies

  • Ability to work independently while managing multiple priorities and deadlines.

  • Strong stakeholder management and cross-functional collaboration skills.

  • High level of accountability, organization, and scientific rigor.


Why Join Syneos Health

  • Contribute to publications supporting over 94% of novel FDA-approved drugs and 95% of EMA-authorized products.

  • Work on high-impact global clinical studies across multiple therapeutic areas.

  • Flexible remote working model with strong career development and training opportunities.

  • Inclusive, diverse, and people-focused global work culture.


About Syneos Health

Syneos Health is a fully integrated biopharmaceutical solutions organization with more than 29,000 professionals across 110+ countries. The company partners with biopharma innovators to accelerate the development and commercialization of life-changing therapies worldwide.


Additional Information

  • Responsibilities may evolve based on business needs.

  • Equivalent experience and qualifications may be considered.

  • Syneos Health is an equal opportunity employer committed to diversity, inclusion, and accessibility.