Senior Medical Writer – Medical Communication Writing
Updated: February 3, 2026
Location: Gurgaon, Haryana, India
Job ID: 25104933-OTHLOC-5206-2DH
Employment Type: Full-Time
About Syneos Health
Syneos Health® is a leading global biopharmaceutical solutions organization dedicated to accelerating customer success. By integrating clinical development, medical affairs, and commercial expertise, Syneos Health delivers innovative, patient-centered solutions that address today’s complex healthcare challenges.
With more than 29,000 professionals across 110 countries, Syneos Health is driven by a shared mission to shorten the distance from lab to life through scientific excellence, collaboration, and operational agility.
Role Overview
The Senior Medical Writer – Medical Communication Writing is responsible for developing high-quality scientific and medical communication deliverables in support of publications, congresses, and medical affairs activities. This role serves as a subject matter expert and project lead, providing scientific leadership, mentoring junior writers, and acting as a primary technical contact for internal stakeholders and clients.
This position is well-suited for experienced medical writers with strong expertise in literature analysis, data interpretation, publication standards, and medical communication strategy.
Key Responsibilities
Medical Communication & Content Development
Conduct comprehensive clinical and scientific literature searches using PubMed and other subscription-based databases.
Critically evaluate, validate, and synthesize scientific references for accuracy, relevance, and compliance.
Develop, review, and update medical communication materials, including slide decks, scientific posters, infographics, newsletters, and other scientific assets.
Ensure all deliverables adhere to client templates, journal or congress guidelines, branding standards, and internal SOPs.
Project Leadership & Collaboration
Act as lead medical writer on assigned projects, managing timelines, deliverables, and quality with minimal supervision.
Coordinate medical writing activities across cross-functional teams and departments.
Mentor and guide junior and mid-level medical writers on complex assignments.
Identify risks, issues, and process gaps during content development and proactively propose solutions or escalations.
Review & Quality Assurance
Serve as a peer reviewer, providing scientific, editorial, and compliance-focused feedback on draft and final documents.
Review deliverables for scientific accuracy, data integrity, referencing quality, appropriate tone, and consistency.
Maintain up-to-date knowledge of global publication standards, regulatory guidelines, and industry best practices.
Tools, Systems & Compliance
Utilize publication planning and content management tools such as Datavision, PubConnect, and Veeva Vault Promomats.
Apply familiarity with data visualization and figure development tools, including GraphPad Prism and Adobe Illustrator, to support high-quality scientific graphics.
Ensure compliance with company SOPs, client standards, and regulatory requirements throughout the writing lifecycle.
Operational Responsibilities
Manage assigned projects within approved budgets and timelines, communicating any changes to leadership proactively.
Complete required administrative and compliance-related tasks within defined timelines.
Perform additional responsibilities as assigned; minimal travel may be required (less than 25%).
Required Qualifications
Education
Advanced degree in Life Sciences, Pharmacy, Medicine, or a related scientific discipline (PhD, MD, PharmD, M.Pharm, MSc preferred)
Experience
Minimum 6–8 years of experience in medical writing or medical communications
Proven experience in publication writing, congress materials, and medical affairs deliverables
Prior experience working with global clients, CROs, or pharmaceutical companies preferred
Technical & Professional Skills
Strong expertise in clinical literature analysis and scientific storytelling
In-depth knowledge of journal and congress publication standards
Proficiency in medical communication tools, publication planning systems, and MS Office
Excellent command of written English with strong editing and review capabilities
Ability to manage multiple projects, priorities, and stakeholders effectively
Soft Skills
Strong leadership, mentoring, and interpersonal skills
High attention to detail and commitment to scientific accuracy
Ability to work independently and collaboratively in a global, matrixed environment
Why Join Syneos Health
Global exposure across high-impact medical communication projects
Structured career development and leadership opportunities
Inclusive, people-first culture with strong learning support
Opportunity to contribute to therapies impacting patients worldwide
Over the past five years, Syneos Health has supported:
94% of all novel FDA-approved drugs
95% of EMA-authorized products
200+ studies across 73,000 sites and more than 675,000 trial participants
Additional Information
The responsibilities listed are not exhaustive and may evolve based on business needs. Syneos Health is an equal opportunity employer and is committed to compliance with all applicable employment, diversity, and accessibility regulations. Reasonable accommodations will be provided in accordance with applicable laws.
Apply now to advance your career as a Senior Medical Writer within a globally recognized biopharmaceutical organization.
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