- Clinical research jobs
- Study Start-Up Opportunities – PhD/Post-Doc Experience
Study Start-Up Opportunities – PhD/Post-Doc Experience
Medpace Holdings, Inc.
United States, OH, Cincinnati | United States, CO, Denver | United States, TX, Irving (Dallas)
Job Summary
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.
Responsibilities
- 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.
Qualifications
- 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.
Job posted: 2024-01-05