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Medical Writer Ii (Scientific Writer +Veeva Vault)

Syneos Health
Syneos Health
3-6 years
preferred by company
10 Jan. 12, 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

Medical Writer II – Scientific Writing (Veeva Vault)

Location: Gurugram, India (Hybrid)
Employment Type: Full-Time
Experience Required: 3–6 Years
Job ID: 25104730
Last Updated: January 8, 2026


About Syneos Health

Syneos Health® is a global, fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success. By combining clinical development, medical affairs, and commercial expertise, Syneos Health transforms complex scientific insights into impactful outcomes that address today’s evolving healthcare landscape.

With a presence in more than 110 countries and a workforce of over 29,000 professionals, Syneos Health places patients and customers at the core of its Clinical Development model, continuously improving efficiency, collaboration, and innovation across global projects.


Job Overview

The Medical Writer II – Scientific Writing (Veeva Vault) role supports clinical, regulatory, and publication teams by delivering high-quality scientific and medical content for global healthcare clients. This hybrid position is ideal for experienced medical writers with hands-on expertise in Veeva Vault, publication workflows, and regulatory-compliant scientific documentation.


Key Responsibilities

  • Serve as a medical writer on clinical study, regulatory, and publication project teams

  • Execute end-to-end scientific writing processes, including workflow management in PubConnect and Veeva Vault

  • Support publication planning activities such as author coordination, approvals, pre-submission queries, and submission execution

  • Compile, write, edit, and coordinate scientific documents with minimal supervision

  • Manage document lifecycle activities including placeholders, version uploads, reference linking, anchoring, and workflow tracking

  • Develop and support scientific deliverables including:

    • Clinical journal manuscripts

    • Scientific abstracts

    • Conference posters and oral presentations

  • Review statistical analysis plans and tables, figures, and listings for scientific accuracy, clarity, formatting, and consistency

  • Collaborate cross-functionally with biostatistics, data management, regulatory affairs, and medical affairs teams

  • Act as a peer reviewer, addressing review comments to ensure scientific integrity and regulatory compliance

  • Ensure adherence to journal and congress guidelines, company SOPs, client standards, and approved templates

  • Conduct online clinical literature searches to support evidence-based content development

  • Utilize publication and document management platforms such as Datavision, PubConnect, and Veeva Vault (PromoMats or MedComms)

  • Maintain awareness of evolving regulatory guidance and industry best practices in medical writing

  • Monitor project budgets and timelines, escalating risks or changes as needed

  • Complete administrative and compliance-related 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

  • 3–6 years of experience in medical writing, scientific writing, or publication development

  • Hands-on experience with Veeva Vault, PubConnect, or similar publication management systems

  • Strong experience in writing and coordinating clinical and scientific documents

  • Solid understanding of journal, congress, and regulatory guidelines

  • Excellent written and verbal communication skills in English

  • High attention to detail with strong organizational and project management capabilities

  • Ability to work effectively in a hybrid, cross-functional, and global team environment


Why Join Syneos Health

  • Hybrid work model with global exposure

  • Opportunity to work on high-impact clinical and scientific publications

  • Structured career development, mentoring, and technical training programs

  • Inclusive, collaborative, and people-first work culture

  • Competitive compensation and comprehensive benefits


Global Impact of Syneos Health

Over the past five years, Syneos Health has supported:

  • 94% of novel FDA-approved drugs

  • 95% of EMA-authorized products

  • More than 200 studies across 73,000 sites and 675,000+ clinical trial patients


Equal Opportunity Statement

Syneos Health is an Equal Opportunity Employer committed to fostering diversity, equity, and inclusion. All employment decisions are based on business needs, qualifications, and merit, without discrimination of any kind.