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Medical Editor Ii Clin Pharm (Editing Of Csr, Ib, Protocol)

Syneos Health
Syneos Health
0-2 years
Not Disclosed
10 Jan. 7, 2026
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

Medical Editor II – Clinical Pharmacology

Location: India – Remote
Job Type: Full-Time
Job ID: 25104357
Updated: December 22, 2025

About Syneos Health

Syneos Health® is a fully integrated biopharmaceutical solutions organization that accelerates customer success by translating clinical, medical affairs, and commercial insights into impactful outcomes. With 29,000 employees across 110 countries, we foster a collaborative and inclusive environment that drives innovation in healthcare.

Position Overview

The Medical Editor II – Clinical Pharmacology ensures the quality, compliance, and accuracy of clinical documents including Clinical Study Reports (CSR), Investigator Brochures (IB), and Protocols. This role provides copyediting, quality review, and document management with minimal supervision to maintain content integrity and regulatory compliance.

Key Responsibilities

Document Editing & Quality Control:

  • Copyedit clinical documents following AMA Manual of Style, internal checklists, and custom client style guidelines.

  • Perform quality reviews of CSRs, IBs, protocols, and other medical writing deliverables to ensure accuracy and regulatory compliance.

  • Maintain familiarity with FDA, EMA, and other regulatory guidelines to ensure documents meet or exceed standards.

Project & Team Collaboration:

  • Represent the editorial group in medical writing and cross-departmental project teams as needed.

  • Monitor project timelines and budgets, updating lead medical writers, project managers, or supervisors on deliverable risks.

  • Provide feedback to lead medical writers regarding the progress and quality of editorial processes.

Process & Compliance:

  • Manage assigned projects according to medical writing SOPs and client standards, ensuring timely and on-budget delivery.

  • Compile medical writing deliverables, ensuring consistency, clarity, and regulatory readiness.

  • Interact with medical writing leadership and staff regarding assigned deliverables as appropriate.

Required Qualifications

  • Undergraduate degree in life sciences, pharmacy, or equivalent experience.

  • Proven experience in copyediting and quality review of clinical documents (CSRs, IBs, protocols).

  • Strong understanding of regulatory standards (FDA, EMA) and industry best practices.

  • Excellent written and verbal communication skills in English.

  • Ability to work independently and manage multiple priorities with minimal supervision.

Why Join Syneos Health

  • Work on high-impact clinical trial documents that contribute to patient care globally.

  • Collaborate with a diverse and inclusive professional team.

  • Access career development, mentorship, and growth opportunities.

  • Join a company dedicated to innovation, quality, and operational excellence in clinical development.