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Sr Medical Editor

0-2 years
Not Disclosed
10 May 2, 2025
Job Description
Job Type: Remote Education: 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

Job Title:

 

Senior Medical Editor


Company:

Syneos Health
A global biopharmaceutical solutions organization delivering integrated clinical and commercial services.


Location:

Gurugram, India (Hybrid, Asia-Pacific Region)


Job ID:

25003003-IND002


Updated:

April 27, 2025


Job Summary:

The Senior Medical Editor ensures the quality, accuracy, and regulatory compliance of clinical and medical documents through rigorous copyediting and data integrity review. The role involves leadership in medical editing activities, project oversight, mentoring, and document management in accordance with regulatory and company standards.


Key Responsibilities:

  • Ensure compliance with FDA, EU, ICH, and other regulatory standards.

  • Represent the editorial team on study and cross-functional project teams.

  • Lead and manage complex or large-scale medical writing projects.

  • Monitor and communicate project timelines, risks, and budgets.

  • Provide training, mentorship, and technical guidance to medical editing and writing staff.

  • Conduct copyediting using AMA style and internal checklists.

  • Perform data integrity reviews to ensure document accuracy.

  • Contribute to development and improvement of SOPs and editorial tools.

  • Compile, publish, and finalize medical documents as needed.

  • Edit SOPs and business documents under the Asset Writing team.


Qualifications:

  • Bachelor’s degree preferred in life sciences, clinical sciences, English, journalism, or related fields.

  • Strong copyediting and publishing experience; Adobe Acrobat or ISIToolbox preferred.

  • Familiarity with AMA style is highly preferred.

  • Strong grammar, detail orientation, and organizational skills.

  • Excellent communication and teamwork abilities.

  • Ability to manage multiple assignments independently and meet deadlines.

  • Knowledge of FDA, EU, ICH, and ISO standards related to regulatory writing is a plus.

  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).


About Syneos Health:

With 29,000 employees in over 110 countries, Syneos Health is a trusted partner to biopharma companies, having supported over 94% of all FDA-approved drugs in the last five years. They promote a culture of inclusion, authenticity, and innovation with strong career growth opportunities.