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Sr Medical Writer (Csr, Ib, Protocol) |Homebased India|

2+ years
Not Disclosed
10 March 3, 2025
Job Description
Job Type: Full Time Education: BA/B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Sr Medical Writer (CSR, IB, Protocol) | Homebased India

Updated: February 13, 2025
Location: India-Asia Pacific - IND-Gurugram-DLF Downtown
Job ID: 25001430

Job Title: Senior Medical Writer

Company: Syneos Health

About Syneos Health:

Syneos Health® is a fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success. Our Clinical Development model prioritizes both customers and patients, simplifying operations and enhancing efficiency. With 29,000 employees across 110 countries, we collaborate to drive innovation and improve lives.

Why Syneos Health?

  • Career development, training, and progression opportunities.
  • Supportive and engaged line management.
  • A culture that values diversity, inclusion, and belonging.
  • Recognition through our Total Rewards Program.

Job Responsibilities:

  • Mentor and lead junior medical writers on complex projects.
  • Act as a lead for assigned writing projects.
  • Manage medical writing activities for individual studies across departments.
  • Develop/support documents including:
    • Clinical study protocols and amendments
    • Clinical study reports
    • Patient narratives
    • Clinical development plans
    • IND submissions and annual reports
    • Integrated summary reports
    • NDA and (e)CTD submissions
    • Investigator brochures
    • Clinical journal manuscripts and abstracts
    • Client presentations
  • Identify and resolve issues during the writing process.
  • Review statistical analysis plans and specifications for accuracy.
  • Collaborate with data management, biostatistics, regulatory, and medical affairs teams.
  • Serve as a peer reviewer on internal teams.
  • Ensure compliance with ICH-E3 guidelines, company SOPs, and client standards.
  • Conduct clinical literature searches when required.
  • Maintain knowledge of industry regulations and guidelines.
  • Manage projects within budgeted hours, reporting any deviations.
  • Perform additional duties as assigned, with minimal travel (<25%).

Qualifications:

  • Bachelor’s degree in Science, English, Communications, or related fields with relevant experience.
  • Strong knowledge of English grammar, FDA, and ICH regulations.
  • Familiarity with AMA style guide.
  • High level of independence, leadership, and team-oriented approach.
  • Proficiency in Microsoft Word, Excel, PowerPoint, email, and Internet.
  • Ability to interpret and present clinical data and complex information.

About Syneos Health’s Impact:

  • Worked on 94% of all Novel FDA Approved Drugs in the past five years.
  • Supported 95% of EMA Authorized Products.
  • Conducted 200+ studies across 73,000 sites with 675,000+ trial patients.

Additional Information:

  • Responsibilities may change at the company’s discretion.
  • Equivalent experience, skills, and education will be considered.
  • Syneos Health complies with EEO and ADA requirements, ensuring fair employment practices.