Medical Writer (Core Labs)

Roles & Responsibilities
• Generate, revise, and maintain clinical and regulatory documents for Core Labs projects
• Coordinate quality control reviews of documents and maintain complete audit trails of revisions and approvals
• Collaborate with internal teams to ensure document accuracy, consistency, and compliance with applicable standards
• Provide input on data analysis planning and assess its impact on clinical document outcomes
• Support cross-functional teams by delivering high-quality documentation within defined timelines
• Perform additional documentation-related duties as assigned to support project and organizational needs

Qualification
• Master’s degree in a health, life sciences, or science-related discipline

Experience
• Suitable for early to mid-level professionals with clinical documentation exposure
• Experience in clinical research, CRO, or laboratory documentation preferred

Skills
• Strong written and verbal communication skills
• Intermediate knowledge of medical terminology and clinical patient management
• Ability to manage multiple documents and maintain version control
• High attention to detail and quality standards
• Ability to work collaboratively in a team-based office environment

About the Company
Medpace is a full-service global clinical contract research organization providing Phase I–IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. With operations across more than 40 countries and deep therapeutic expertise, Medpace supports the development of safe and effective medical therapies through a disciplined, science-driven approach.