Senior Medical Writer – Scientific Writing & Veeva
Location: India (Remote)
Employment Type: Full-Time
Experience Required: 6–10 Years
Job ID: 25104930
Last Updated: January 8, 2026
About the Company
Syneos Health® is a leading global biopharmaceutical solutions organization, partnering with customers to accelerate the successful development and commercialization of innovative therapies. With operations across 110+ countries and a workforce of over 29,000 professionals, Syneos Health integrates clinical development, medical affairs, and commercial expertise to address today’s evolving healthcare landscape.
Driven by a patient-centric Clinical Development model, Syneos Health continuously simplifies and optimizes processes to deliver high-quality outcomes while fostering an engaging and collaborative work environment.
Job Summary
The Senior Medical Writer (Scientific Writing + Veeva) will serve as a key contributor on clinical, regulatory, and publication project teams. This role involves writing, editing, and coordinating complex scientific documents while acting as the primary technical liaison between internal stakeholders and clients. The position offers the flexibility of remote work while collaborating with global cross-functional teams.
Key Responsibilities
Lead and mentor junior medical writers on complex scientific and publication projects
Act as the primary medical writing lead for assigned studies and deliverables
Manage end-to-end medical writing activities with minimal supervision
Develop, review, and finalize scientific documents including:
Clinical journal manuscripts and abstracts
Scientific posters and oral presentations
Review statistical analysis plans and table, figure, and listing specifications for accuracy, clarity, and consistency
Ensure compliance with journal, congress, regulatory, and company-specific guidelines, SOPs, and approved templates
Conduct online clinical literature searches to support scientific content development
Collaborate closely with biostatistics, data management, regulatory affairs, and medical affairs teams
Perform peer reviews to ensure scientific accuracy, data integrity, referencing quality, and appropriate branding
Utilize publication planning and document management tools such as Veeva Vault (Promomats), Datavision, and PubConnect
Develop high-quality scientific figures using tools such as GraphPad Prism and Adobe Illustrator
Monitor project timelines and budgets, communicating risks or changes proactively
Stay current with evolving regulatory requirements and global medical writing standards
Complete required administrative tasks within defined timelines
Minimal travel may be required (less than 25%).
Required Qualifications
Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Medicine, or a related scientific discipline
6–10 years of professional experience in medical writing, scientific publications, or regulatory writing
Strong experience with clinical publications and scientific content development
Hands-on experience with Veeva Vault and publication planning systems
Excellent written and verbal English communication skills
Strong attention to detail with the ability to manage multiple projects under tight deadlines
Proven ability to work effectively in cross-functional and global team environments
Why Join Syneos Health
Opportunity to work remotely with a globally recognized biopharmaceutical organization
Exposure to high-impact clinical and scientific projects across therapeutic areas
Structured career development, technical training, and mentoring programs
Inclusive and diverse workplace culture focused on professional growth and well-being
Competitive compensation and comprehensive benefits
About Syneos Health Impact
In the past five years, Syneos Health has partnered on:
94% of all novel FDA-approved drugs
95% of EMA-authorized products
200+ studies across 73,000 sites and 675,000+ trial patients
Equal Opportunity Statement
Syneos Health is an Equal Opportunity Employer and is committed to fostering an inclusive and diverse workplace. Employment decisions are based solely on business needs, qualifications, and merit, without discrimination of any kind.
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