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Senior Medical Writer (Medical Information Writing)

Syneos Health
Syneos Health
5-8 years
Not Disclosed
Gurugram, India
10 March 24, 2026
Job Description
Job Type: Full Time Hybrid 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 – Medical Information Writing

Location: Gurugram, India (Hybrid)
Job Type: Full-Time
Industry: Medical Writing / Clinical Research / Medical Affairs
Company: Syneos Health
Experience Required: 5–8 years in medical writing or medical information

Job Overview
Syneos Health is seeking an experienced Senior Medical Writer – Medical Information Writing to support global medical information and scientific communication activities. This role involves leading complex writing projects, developing scientifically accurate content, and responding to medical queries from healthcare professionals, patients, and internal stakeholders. The position requires strong expertise in medical writing, literature analysis, and regulatory compliance within a fast-paced, global environment.

Key Responsibilities
Lead and mentor junior medical writers while managing complex medical information writing projects independently. Develop, review, and update global standard scientific response documents (gSSRCs), FAQs, and other medical information materials in line with client templates and style guides. Respond to escalated medical queries from healthcare professionals, patients, and internal stakeholders with scientifically accurate and compliant information. Conduct comprehensive literature searches using databases such as PubMed and validate relevant scientific data for inclusion in deliverables. Create and support the development of clinical manuscripts, abstracts, posters, and presentations for scientific dissemination. Ensure all documents meet regulatory standards, journal guidelines, and company SOPs while maintaining high quality, accuracy, and consistency.

Collaborate cross-functionally with teams in data management, biostatistics, regulatory affairs, and medical affairs to deliver high-quality scientific content. Perform peer review of documents to ensure scientific accuracy, appropriate referencing, and adherence to branding and style guidelines. Utilize tools such as GraphPad Prism and Adobe Illustrator for data visualization and figure creation. Work with publication planning tools such as Datavision and Veeva Vault PromoMats for content management and tracking. Identify and resolve writing-related challenges, ensuring timely delivery of projects within budget constraints. Maintain awareness of evolving industry practices, regulatory requirements, and medical writing standards.

Eligibility Criteria
Master’s degree or higher in Life Sciences, Pharmacy, Medicine, or a related field is required. Candidates should have 5–8 years of experience in medical writing, with a strong focus on medical information, publications, or regulatory writing.

Required Skills and Competencies
Strong expertise in medical and scientific writing, including development of medical information responses and publication materials. Excellent literature review and data interpretation skills. In-depth understanding of global regulatory requirements, publication guidelines, and scientific communication standards. Proficiency in literature databases such as PubMed. Experience with data visualization and figure creation tools. Familiarity with publication and content management platforms such as Veeva Vault and Datavision is preferred. Strong attention to detail, quality, and accuracy. Excellent written and verbal communication skills. Ability to manage multiple projects and work collaboratively in cross-functional teams.

Why Join Syneos Health
Syneos Health offers a collaborative and innovation-driven work environment with opportunities to work on global medical communication projects. Employees benefit from structured career development programs, continuous learning opportunities, and exposure to cutting-edge clinical and medical affairs initiatives.

Equal Opportunity Statement
Syneos Health is an equal opportunity employer committed to fostering a diverse and inclusive workplace. All qualified applicants will receive equal consideration for employment in accordance with applicable laws and regulations.

This role is ideal for experienced medical writers looking to advance their careers in medical information writing, scientific communications, and global healthcare content development.