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Medical Writer I

0-2 years
Not Disclosed
10 Sept. 22, 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

Job Title:

Medical Writer I

Location: IND-Gurugram
Job ID: 25101794
Updated: September 18, 2025


Company Overview – Syneos Health

Syneos Health® is a fully integrated biopharmaceutical solutions organization focused on accelerating customer success. The company emphasizes patient-centric clinical development while streamlining processes to ensure efficiency and high-quality outcomes.

Key Highlights:

  • Operates in 110 countries with 29,000 employees.

  • Partnered with 94% of Novel FDA Approved Drugs, 95% of EMA Authorized Products, 200+ studies, 73,000 sites, and 675,000+ trial patients in the last 5 years.

  • Promotes career development, technical training, and peer recognition.

  • Fosters a diverse, inclusive, and authentic workplace through its Total Self culture.

Learn more: Syneos Health


Role Summary

The Medical Writer I supports clinical and regulatory projects by compiling, writing, and editing medical documents. Works under moderate supervision and collaborates across departments to ensure high-quality, timely deliverables.


Key Responsibilities

  • Compile, write, and edit clinical and regulatory documents, including:

    • Clinical study protocols and amendments

    • Clinical study reports

    • Patient narratives

    • Investigator brochures

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

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

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

  • Perform online clinical literature searches as applicable.

  • Monitor project budgets and work within allocated hours.

  • Complete administrative tasks and other assigned duties.

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

  • Continually develop professional knowledge to stay current with regulatory guidance and client expectations.


Candidate Profile / Skills

  • Education: Bachelor of Science (with relevant writing experience) or Bachelor of Arts (Social Sciences, English, Communications) with scientific/medical knowledge.

  • Strong knowledge of English grammar and AMA style guide.

  • Understanding of FDA and ICH regulations and guidelines preferred.

  • Strong presentation, proofreading, interpersonal, and team collaboration skills.

  • Proficiency in Microsoft Word, Excel, PowerPoint, email, and internet tools.

  • Ability to interpret clinical data and present complex information clearly.


Additional Information

  • Tasks listed are not exhaustive; the company may assign additional duties.

  • Equivalent skills or experience may be considered in lieu of formal qualifications.

  • Nothing in this description constitutes an employment contract.

  • Syneos Health is committed to ADA compliance and providing reasonable accommodations.


How to Apply

  • Apply directly via Syneos Health website.

  • Not ready to apply? Join the Talent Network to stay connected for future opportunities.