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Medical Writer I

0-2 years
Not Disclosed
10 Sept. 24, 2025
Job Description
Job Type: Full Time 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 I – Syneos Health

Location: Gurugram, India
Job ID: 25101794
Updated: September 18, 2025


About Syneos Health

Syneos Health® is a fully integrated biopharmaceutical solutions organization focused on accelerating clinical development and improving patient outcomes.

  • Employees: 29,000 across 110 countries

  • Experience: Worked with 94% of Novel FDA-approved drugs, 95% of EMA-authorized products, 200+ studies, 73,000 sites, and 675,000+ trial patients.

  • Culture: Total Self culture fostering diversity, authenticity, career growth, and inclusion.


Job Overview

The Medical Writer I contributes to clinical and regulatory documentation under moderate supervision. Responsibilities include writing, reviewing, and editing documents, coordinating with cross-functional teams, and ensuring compliance with regulatory and company standards.


Key Responsibilities

Medical Writing & Documentation:

  • Write, compile, and edit medical writing deliverables including:

    • Clinical study protocols and amendments

    • Clinical study reports

    • Patient narratives

    • Investigator brochures

  • Review statistical analysis plans and table/figure/listing specifications for content, format, and consistency.

  • Conduct online clinical literature searches as needed.

Collaboration & Coordination:

  • Interact with teams including data management, biostatistics, regulatory affairs, and medical affairs to produce accurate deliverables.

  • Ensure alignment with client and company standards, templates, and timelines.

Compliance & Quality:

  • Adhere to regulatory standards (e.g., ICH-E3), SOPs, and client-specific guidelines.

  • Maintain high-quality, on-time, and on-budget deliverables.

Professional Development:

  • Stay updated on regulatory guidance and best practices in medical writing.

  • Understand and work within project budgets; report changes to leadership.

Other Duties:

  • Complete administrative tasks and perform other duties as assigned.

  • Minimal travel required (<25%).


Qualifications & Requirements

  • Education:

    • BSc with relevant writing experience or BA (Social Sciences, English, Communications) with scientific/medical knowledge.

  • Experience & Skills:

    • Knowledge of English grammar and AMA style guide.

    • Familiarity with FDA and ICH regulations preferred.

    • Strong proficiency in Word, Excel, PowerPoint, email, and Internet.

    • Ability to interpret and present clinical data.

    • Effective proofreading, presentation, and interpersonal skills.

    • Team-oriented mindset.


Additional Information

  • Tasks and responsibilities may vary at company discretion.

  • Equivalent experience, skills, or education may be considered.

  • Compliance with ADA and diversity/inclusion policies.

  • Expressing interest adds you to Syneos Health’s talent pipeline for future opportunities.