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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: Gurugram, India – Hybrid

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

Syneos Health is hiring a Senior Medical Editor to oversee editing and quality control of regulatory and clinical documents. This role is ideal for experienced professionals in medical writing, copyediting, and publishing who are passionate about ensuring compliance, accuracy, and excellence in regulatory documentation for global pharmaceutical clients.

Responsibilities:

  • Edit and perform QC of regulatory documents including clinical study protocols, CSRs, Investigator’s Brochures, and Module 2 clinical summaries.

  • Review manuscripts, abstracts, and posters for accuracy, grammar, formatting, and compliance with AMA or sponsor-specific style guides.

  • Conduct data integrity checks to ensure precision and compliance with FDA, EMA, and ICH guidelines.

  • Mentor and train medical editors and writers on best practices, style, and data integrity standards.

  • Act as project lead on large or complex deliverables, ensuring timelines and budgets are met.

  • Represent the editorial function in cross-functional study and project team meetings.

  • Contribute to process improvement initiatives and SOP updates.

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

Required Skills & Qualifications:

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

  • Minimum 5 years of medical editing or publishing experience in pharma or CRO environment.

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

  • Proven experience in QC review of regulatory documents and publication deliverables.

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

  • Excellent communication, problem-solving, organizational, and project management skills.

  • Knowledge of FDA, EMA, ICH, and ISO regulatory document requirements preferred.

  • Ability to manage multiple assignments independently and adapt to changing priorities.

Perks & Benefits:

  • Competitive compensation package with performance-based rewards.

  • Hybrid working model in Gurugram, combining flexibility with collaboration.

  • Global exposure to top pharmaceutical sponsors and regulatory projects.

  • Career development, training programs, and mentorship opportunities.

  • Supportive work culture driven by diversity, inclusion, and recognition.

Company Overview:
Syneos Health is a leading biopharmaceutical solutions organization with over 29,000 employees across 110 countries. Partnering with 94% of FDA-approved drugs and 95% of EMA-authorized products in the past five years, Syneos Health accelerates clinical development and ensures regulatory excellence worldwide.

Work Model: Hybrid – Gurugram, India

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

Apply now to join Syneos Health as a Senior Medical Editor and play a key role in ensuring the accuracy and compliance of regulatory documents for global clinical trials.