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Medical Writer Ii (Scientific Writer +Veeva Vault)

Syneos Health
Syneos Health
0-2 years
Not Disclosed
10 Jan. 13, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

Medical Writer II – Scientific Writing & Veeva Vault
Location: Gurugram, India (Hybrid) | Job ID: 25104730 | Employment Type: Full-Time

About Syneos Health
Syneos Health® is a leading fully integrated biopharmaceutical solutions organization, dedicated to accelerating clinical development and delivering impactful patient outcomes. Our teams combine clinical, medical affairs, and regulatory expertise to create innovative solutions that address the evolving landscape of healthcare and science.

With 29,000 employees across 110 countries, we prioritize collaboration, continuous learning, and excellence in delivering therapies that make a real difference.

Role Overview
The Medical Writer II plays a key role in clinical, regulatory, and publication projects, contributing to scientific writing, document preparation, and quality review. This role leverages Veeva Vault (PubConnect/PromoMats) to manage workflows, author approvals, and publication submissions while collaborating across functional teams to ensure timely and high-quality deliverables.

Key Responsibilities

  • Write, edit, and coordinate clinical, regulatory, and scientific documents with minimal supervision.

  • Mentor junior writers and provide guidance on project deliverables as needed.

  • Manage end-to-end publication workflows including PubConnect, publication planning, author approvals, pre-submission queries, and submission activities.

  • Develop and review clinical journal manuscripts, abstracts, posters, and oral presentations.

  • Review statistical analysis plans and tables/figures/listings for scientific accuracy, formatting, grammar, and consistency.

  • Collaborate with data management, biostatistics, regulatory affairs, and medical affairs teams to finalize deliverables.

  • Serve as peer reviewer, addressing comments to ensure content clarity, consistency, and scientific accuracy.

  • Perform literature searches and adhere to congress/journal guidelines, company SOPs, client standards, and approved templates.

  • Monitor project budgets and timelines, communicating changes to medical writing leadership.

  • Perform administrative tasks and project tracking within required timeframes.

  • Minimal travel (<25%) may be required.

Qualifications & Experience

  • Bachelor’s degree in Life Sciences, Pharmacy, English, Communications, or related field.

  • Proven experience in medical writing for clinical, regulatory, or publication projects.

  • Proficiency with Veeva Vault (PubConnect/PromoMats) and publication planning tools such as Datavision.

  • Strong knowledge of FDA/ICH regulations, journal/congress guidelines, and AMA style.

  • Excellent written, verbal, and interpersonal communication skills.

  • Ability to collaborate cross-functionally and mentor junior staff.

  • Familiarity with managing publication workflows and document version control.

Why Join Syneos Health

  • Work on global scientific publications and regulatory writing projects.

  • Collaborate with multi-disciplinary teams in a supportive, inclusive environment.

  • Contribute to projects that impact patient care worldwide.

  • Access career development, training programs, and mentorship opportunities.

Apply Now
Join Syneos Health as a Medical Writer II and contribute to high-quality scientific communications that advance global healthcare and clinical research.