Medical Writer

Responsibilities

• Write, edit, and maintain high-quality, complex clinical and regulatory documents, including clinical study reports, protocols, Investigator’s brochures, and IND/NDA modules
• Coordinate and conduct quality control reviews
• Effectively communicate and collaborate with Sponsors and Medpace subject matter experts
• Manage multiple projects and tasks simultaneously while meeting strict deadlines
• Maintain compliance with company processes, industry guidelines, and regulations

Requirements

• PhD in Life Sciences with a focus in Cardiovascular and/or Metabolic research (clinical or nonclinical)
• Ability to synthesize complex information into a clear and concise format for target audiences
• Strong analytical skills and scientific writing capabilities
• Self-motivated, energetic, and eager to learn in a professional environment

Preferred Qualifications

• Prior experience in the CRO, pharmaceutical, or medical writing industries

Benefits

• Competitive compensation and benefits package
• Competitive PTO packages starting at 20+ days
• Structured career paths with professional growth opportunities
• Modern, eco-friendly campus with an on-site fitness center
• Employee health and wellness initiatives
• Discounted tuition for UC online programs

About the Company

Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, we leverage therapeutic expertise across major areas including oncology, cardiology, and metabolic disease to accelerate the global development of safe and effective medical therapeutics.