Study Start-Up Project Manager (Cincinnati)

Do you enjoy working in a fast-paced environment where you are empowered to make strategic decisions and contribute to a growing and profitable company? Join us at Medpace! Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Global Study Start-Up Project Manager to join our Clinical Operations team. This position plays a key role in the clinical trial management process at Medpace. 

Incentives can include: Competitive bonus program, sign-on/relocation bonus, and equity awards.

Location: Position is office based in Cincinnati, OH.

• Efficiently manage successful execution of global start-up, maintenance, and close-out studies;
• Effectively lead others in a matrix environment;
• 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;
• Review pertinent regulations to develop proactive solutions to start-up challenges;
• Prepare new business proposals and present during bid defenses, general capabilities meetings, and audits;
• Contribute to the growth and development of departmental staff, processes and systems.

• Bachelor's degree required, advanced degree in Life Sciences preferred
• Experience with Cardiovascular and Metabolic indications in an academic and/or clinical trial setting is desired, such as, but not limited to, NASH, diabetes, medical devices and coronary artery diseases.
• 5+ years of experience in clinical research, preferably in a Senior/Lead role at a CRO in Study Start-Up
• Project management experience and demonstrated role in developing others
• Strong oral and written communication skills required

Travel: Minimal