Senior Medical Writer – Scientific Writing & Veeva Experience
Location: Gurugram, India (Hybrid)
Employment Type: Full-time
Job ID: 25104930
Last Updated: January 8, 2026
Job Overview
Syneos Health is a globally recognized biopharmaceutical solutions organization dedicated to accelerating the development and commercialization of innovative therapies. With operations across more than 110 countries, Syneos Health integrates clinical development, medical affairs, and commercial expertise to deliver impactful outcomes for patients and sponsors worldwide.
We are currently seeking an experienced Senior Medical Writer with strong expertise in scientific writing and Veeva-based publication tools to join our growing team in Gurugram. This role offers the opportunity to lead complex medical writing projects, collaborate with global cross-functional teams, and contribute to high-impact clinical and scientific deliverables.
Key Responsibilities
Lead and manage medical writing activities for assigned clinical, regulatory, and publication projects
Serve as the primary medical writing contact for internal stakeholders and clients
Mentor and guide junior and mid-level medical writers on complex assignments
Develop, review, and finalize high-quality scientific documents, including:
Clinical journal manuscripts and abstracts
Posters and oral presentations for congresses
Scientific publications and medical communication materials
Review statistical analysis plans, tables, figures, and listings for scientific accuracy, consistency, and clarity
Ensure compliance with global regulatory requirements, journal and congress guidelines, SOPs, and client standards
Conduct clinical literature searches to support scientific narratives
Collaborate closely with biostatistics, data management, regulatory affairs, and medical affairs teams
Utilize publication planning and document management tools such as Veeva Vault PromoMats, Datavision, and PubConnect
Review content for data integrity, appropriate referencing, branding accuracy, and editorial quality
Maintain awareness of evolving regulatory guidelines and industry best practices
Manage project timelines and budgets, ensuring on-time and high-quality delivery
Perform peer reviews and contribute to continuous quality improvement initiatives
Required Experience and Qualifications
Minimum 6–10 years of experience in medical writing within CROs, pharmaceutical companies, or medical communications agencies
Proven experience in scientific writing, clinical publications, and regulatory documentation
Hands-on experience with Veeva Vault PromoMats and publication planning tools
Strong understanding of clinical research processes and regulatory standards (ICH, GCP, journal guidelines)
Experience reviewing statistical outputs and collaborating with biostatistics teams
Excellent written and verbal communication skills in English
Ability to manage multiple projects independently with minimal supervision
Preferred Skills
Familiarity with data visualization and figure development tools such as GraphPad Prism or Adobe Illustrator
Experience working in global, matrixed team environments
Strong mentoring and leadership capabilities
High attention to detail with strong organizational and problem-solving skills
Why Join Syneos Health
Opportunity to work on the majority of novel FDA- and EMA-approved therapies
Exposure to global clinical research and high-impact scientific projects
Strong focus on professional development, technical training, and career progression
Inclusive, diverse, and people-first work culture
Competitive compensation and comprehensive rewards program
Equal Opportunity Statement
Syneos Health is an Equal Opportunity Employer and is committed to fostering a diverse, inclusive, and equitable workplace. Employment decisions are based on business needs, qualifications, and merit, without discrimination of any kind.
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