Medical Writer – Core Labs
Job ID: 11938
Location: Navi Mumbai, India
Department: Core Laboratories
Employment Type: Full-Time | Office-Based
Industry: Clinical Research / CRO
Experience Required: 2–5 Years
Job Overview
We are seeking a skilled and detail-oriented Medical Writer (Core Labs) to join a rapidly expanding global clinical research organization. Based in Navi Mumbai, this full-time, office-based role will support Core Laboratory operations by developing, reviewing, and maintaining high-quality clinical documentation that contributes directly to successful clinical trial execution.
The ideal candidate will collaborate with cross-functional clinical teams and play a critical role in ensuring document accuracy, regulatory compliance, and data integrity throughout the clinical development lifecycle.
Key Responsibilities
Develop, revise, and maintain clinical and laboratory-related documents in accordance with internal standards and regulatory requirements
Coordinate quality control (QC) activities, ensuring complete audit trails for document reviews, approvals, and revisions
Collaborate with clinical and data teams to provide input on data analysis planning and assess its impact on clinical documentation outcomes
Ensure consistency, accuracy, and clarity across all written scientific and clinical materials
Support internal teams with documentation-related tasks across ongoing clinical projects
Perform additional responsibilities as assigned to support Core Labs and clinical operations
Education & Experience Requirements
Master’s degree in a health, life sciences, or science-related discipline
2 to 5 years of relevant experience in medical writing, clinical documentation, or clinical research environments
Prior exposure to CRO, clinical trials, or laboratory-based documentation is highly preferred
Required Skills & Competencies
Strong written and verbal communication skills with high attention to detail
Intermediate to advanced knowledge of medical terminology and clinical patient management
Understanding of clinical research processes and documentation standards
Ability to work effectively in a team-oriented, deadline-driven environment
Strong organizational skills with the ability to manage multiple tasks simultaneously
About the Organization
Medpace is a global, full-service Clinical Research Organization (CRO) providing Phase I–IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. With expertise across major therapeutic areas including oncology, cardiology, CNS, endocrinology, metabolic diseases, and infectious diseases, Medpace supports the global development of safe and effective medical therapeutics.
Headquartered in Cincinnati, Ohio, the organization employs over 5,000 professionals across more than 40 countries worldwide.
Why Join This Opportunity
Work in a globally recognized CRO with strong scientific and regulatory expertise
Be part of impactful clinical research that improves patient outcomes worldwide
Structured career progression with clear professional growth pathways
Collaborative, purpose-driven work culture focused on quality and innovation
Benefits & Perks
Flexible and supportive work environment
Competitive compensation and comprehensive benefits package
Generous paid time off (PTO)
Structured career development and training opportunities
Employee wellness initiatives and appreciation programs
Awards & Recognition
Recognized by Forbes as one of America’s Most Successful Midsize Companies (2021–2024)
Recipient of multiple CRO Leadership Awards for expertise, quality, reliability, and performance
SEO & GPT-Optimized Keywords
Medical Writer Jobs Navi Mumbai, Core Lab Medical Writing Jobs, CRO Medical Writer India, Clinical Documentation Specialist Jobs, Medical Writing Careers in Clinical Research, Pharma CRO Jobs India
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