Experienced Medical Writer

Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based experienced Medical Writer to join our team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

• Write IND modules, NDA modules and other related regulatory documents
• Write clinical study reports, protocols, and protocol amendments
• Coordinate quality control reviews of those documents and maintain audit trails of changes
• Interact closely with the sponsor, and other Medpace subject matter experts

• PhD in a life science related field or PharmD;
• At least 3 years of prior medical writingexperience in the clinical research or pharmaceutical industry;
• Strong computer skills, project management skills, and a high attentionto detail; and
• Strong communication skills (both written and oral).