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Senior Medical Editor (Editing And Qc Of Regulatory Docs)

5+ years
INR 12–20 LPA
10 Aug. 25, 2025
Job Description
Job Type: Full Time 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

Location: India – Remote

Senior Medical Editor (Editing and QC of Regulatory Docs) – Syneos Health

Syneos Health is seeking an experienced Senior Medical Editor to lead editing and quality control of regulatory and clinical documents. This role is perfect for professionals with strong expertise in medical editing, copyediting, and regulatory publishing who are passionate about supporting global pharmaceutical and clinical research programs.

Responsibilities:

  • Edit and quality-check regulatory documents including clinical study protocols, amendments, CSRs, Investigator’s Brochures, and clinical summaries.

  • Review publication deliverables such as manuscripts, abstracts, and posters for accuracy, grammar, and compliance.

  • Apply AMA style guidelines and sponsor-specific style guides to ensure consistency and quality.

  • Conduct data integrity checks to ensure compliance with regulatory requirements.

  • Provide mentorship and training to junior editors and medical writing teams.

  • Act as project lead for complex editing deliverables, ensuring timelines and budgets are met.

  • Participate in cross-functional meetings and represent the editorial team in project discussions.

  • Support process improvements and contribute to updating editorial SOPs.

  • Compile and publish deliverables as required using Adobe Acrobat, ISIToolbox, and Microsoft Office Suite.

Required Skills & Qualifications:

  • Bachelor’s degree in Life Sciences, Clinical Sciences, English/Journalism, or related field.

  • Minimum 5 years of medical editing or regulatory publishing experience.

  • Strong expertise in editing, copyediting, grammar, punctuation, and style application (AMA or custom guidelines).

  • Experience with QC of regulatory documents and data integrity review.

  • Familiarity with FDA, EMA, ICH regulations, and ISO standards related to regulatory documents.

  • Proficiency in Adobe Acrobat, Microsoft Office Suite, and publishing tools; ISIToolbox preferred.

  • Excellent project management, communication, and organizational skills.

  • Ability to manage multiple projects independently with strict deadlines.

Perks & Benefits:

  • Competitive salary aligned with senior medical editing roles in India.

  • 100% remote work flexibility.

  • Career development, training, and global project exposure.

  • Supportive work culture with mentorship and recognition programs.

  • Opportunity to work with top global pharmaceutical sponsors.

Company Overview:
Syneos Health is a leading biopharmaceutical solutions organization working with 94% of FDA-approved drugs and 95% of EMA-authorized products in the past five years. With 29,000 employees across 110 countries, Syneos Health accelerates clinical research and brings life-changing therapies to patients worldwide.

Work Model: Remote

Expected Salary: Competitive range for Senior Medical Editors in India typically falls between INR 12–20 LPA, depending on experience and expertise.

Apply today to join Syneos Health as a Senior Medical Editor and ensure the highest quality in regulatory documentation for global clinical trials.