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Senior Medical Writer(Scientific Writer & Quality Check)

Syneos Health
Syneos Health
0-2 years
Not Disclosed
10 Jan. 12, 2026
Job Description
Job Type: Full Time Remote 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

Job Title: Senior Medical Writer (Scientific Writing & Quality Control)
Company: Syneos Health
Location: Remote – India
Job ID: 25104933
Updated On: 9 Jan 2026

Company Overview:
Syneos Health® is a global, fully integrated biopharmaceutical solutions organization focused on accelerating clinical development and commercial success. We deliver innovative solutions across clinical development, medical affairs, and commercialization, placing the patient and client at the center of every decision. With 29,000 employees across 110 countries, we combine expertise, agility, and collaboration to improve healthcare outcomes worldwide.

Position Summary:
The Senior Medical Writer will serve as a key contributor to clinical, regulatory, and publication projects. This role involves writing, editing, and coordinating scientific and clinical content while ensuring high-quality, compliant deliverables. The position also includes mentoring junior writers and acting as a technical point of contact within project teams.

Key Responsibilities:

  • Lead medical writing activities for clinical study, regulatory, or publication projects.

  • Mentor and guide less experienced medical writers on complex projects.

  • Develop, edit, and review documents including:

    • Clinical study reports (CSRs)

    • Journal manuscripts, abstracts, posters, and presentations

    • Statistical analysis plans and table/figure/listing specifications

  • Review draft documents for scientific accuracy, grammar, format, and regulatory compliance.

  • Conduct systematic literature searches and data analysis to support document preparation.

  • Collaborate with cross-functional teams including data management, biostatistics, regulatory affairs, and medical affairs.

  • Ensure adherence to company SOPs, client standards, and regulatory guidelines (FDA, ICH, and journal/congress-specific standards).

  • Utilize software tools for data visualization and figure creation (e.g., GraphPad Prism, Adobe Illustrator).

  • Maintain awareness of project budgets and timelines, ensuring efficient and timely delivery.

  • Perform other duties as assigned; minimal travel (<25%) may be required.

Qualifications and Skills:

  • Bachelor of Science (B.Sc.) in Life Sciences, Pharmacy, or related field; or Bachelor of Arts (English, Social Sciences, Communications) with scientific/medical knowledge.

  • Extensive knowledge of English grammar, AMA style guide, and ICH/FDA regulations.

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

  • Strong analytical and data interpretation skills with the ability to present complex clinical information clearly.

  • Proficiency in Microsoft Office (Word, Excel, PowerPoint), email, and internet research.

  • Familiarity with publication planning software (e.g., Datavision, PubConnect, VeevaVault Promomats) is advantageous.

  • Ability to mentor junior staff and manage multiple writing projects independently.

Experience Required:

  • Significant experience in medical writing, regulatory submissions, and scientific publications.

  • Leadership experience on writing projects or peer review of medical writing deliverables.

Why Join Syneos Health:

  • Work remotely with a global team on high-impact clinical development and publication projects.

  • Engage in professional growth through training, mentoring, and cross-functional collaboration.

  • Contribute to innovative, patient-focused solutions in a flexible, inclusive, and supportive work environment.

  • Participate in global projects that influence drug development and healthcare outcomes.