Study Start-Up Opportunities – PhD/Post-Doc Experience

Medpace is seeking PhD graduates for opportunities within our Study Start-Up/Regulatory Submissions group. This is a great opportunity to enter the clinical research industry and receive excellent foundational training!

Position can be located in Cincinnati, Dallas or Denver.

• Collect, review, organize, and assemble regulatory start-up submissions (includes submissions to Institutional Review Boards, or IRB);
• Develop and maintain timelines for study start-up through both internal and external collaboration;
• Collaborate with cross-functional team members for drugs or devices in development
• Utilize a Clinical Trial Management System (CTMS) for daily tasks, oversight, and reporting of trial status
• Review pertinent regulations and guidance to develop proactive solutions to regulatory issues and challenges;
• Perform quality checks on submission documents and site essential documents;
• Prepare and approve informed consent forms;
• Serve as a Sponsor point of contact for start-up and regulatory submissions items; and

• Receive mentorship and training from experienced Study Start-Up Managers and Directors.

• PhD in Life Sciences;
• Clinical Research and project management experience strongly preferred;
• Able to think critically for identification of issues and solutions; and
• Strong oral and written communication skills required.