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Medical Writer (Core Labs)

Medpace
Medpace
0-3 years
preferred by company
10 Jan. 12, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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 Writer – Core Labs

Job ID: 11938
Location: Navi Mumbai, India
Department: Core Labs
Employment Type: Full-Time | Office-Based


Job Overview

Medpace is expanding its global operations and is seeking a skilled Medical Writer (Core Labs) to join its Navi Mumbai office. This role is integral to clinical research documentation and supports global clinical development programs. The Medical Writer will collaborate closely with cross-functional teams to develop, review, and maintain high-quality clinical documents that support regulatory and operational excellence.


Key Responsibilities

  • Develop, review, and maintain clinical research documents in alignment with project requirements and regulatory standards

  • Revise clinical documentation to ensure accuracy, consistency, and compliance throughout the document lifecycle

  • Coordinate quality control reviews and maintain clear audit trails for document revisions and approvals

  • Provide scientific input into data analysis planning and assess its impact on clinical documentation outcomes

  • Collaborate with internal stakeholders to support timely delivery of documentation milestones

  • Ensure adherence to internal SOPs, industry guidelines, and clinical research best practices

  • Perform additional documentation and project-related responsibilities as assigned


Experience Required

  • 0–3 years of experience in medical writing, clinical documentation, or clinical research support roles

  • Experience within a CRO, pharmaceutical, biotechnology, or medical device environment is preferred


Qualifications

  • Master’s degree in a health, life sciences, pharmacy, or related scientific discipline

  • Strong written and verbal communication skills with high attention to detail

  • Working knowledge of medical terminology and clinical patient management concepts

  • Ability to work collaboratively in a team-based, fast-paced clinical research environment


About Medpace

Medpace is a global, full-service clinical contract research organization (CRO) providing Phase I–IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. With more than 5,000 employees across 40+ countries, Medpace leverages deep therapeutic and regulatory expertise across oncology, cardiology, CNS, metabolic diseases, endocrinology, anti-viral, and anti-infective research.


Why Join Medpace

At Medpace, our people are driven by purpose and passion. For over 30 years, our work has contributed to improving the lives of patients worldwide. By joining Medpace, you become part of a mission-focused organization dedicated to advancing safe and effective medical therapies.


Employee Benefits & Perks

  • Flexible and collaborative work environment

  • Competitive compensation and comprehensive benefits package

  • Generous paid time off policies

  • Structured career development and internal growth opportunities

  • Company-sponsored employee recognition and engagement programs

  • Health and wellness initiatives supporting employee well-being


Awards & Recognition

  • Forbes: America’s Most Successful Midsize Companies (2021–2024)

  • CRO Leadership Awards by Life Science Leader for expertise, quality, reliability, and capabilities


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