Study Start-Up Project Manager

Medpace; Cincinnati (OH); On-site; USD 80,000 - 110,000; Full time

Job summary

An established industry player in clinical operations is seeking a Global Study Start-Up Project Manager to oversee critical clinical trial processes. This full-time position involves managing the start-up, maintenance, and close-out of studies while leading teams in a dynamic environment. The role offers exciting incentives, including bonuses and equity awards, and the opportunity to contribute to the growth of departmental staff and processes. If you have a strong background in clinical research and project management, this is a fantastic opportunity to make a significant impact in the field.

Benefits

Sign-on Bonus

Relocation Bonus

Equity Awards

Qualifications

• 5+ years of clinical research experience, preferably in a senior/lead role at a CRO.
• Strong project management and leadership skills are essential.

Responsibilities

• Manage successful execution of global studies and lead teams effectively.
• Perform quality checks on submission documents and serve as sponsor contact.

Skills

Project Management

Clinical Research

Leadership

Communication

Education

Bachelor's Degree

Advanced Degree in Life Sciences

Job description

Study Start-Up Project Manager

Location: United States - OH - Cincinnati

Job Summary

Join Medpace as a Global Study Start-Up Project Manager in our Clinical Operations team. This full-time role is vital for managing clinical trial processes, including start-up, maintenance, and close-out studies. We offer incentives such as bonuses, sign-on/relocation bonuses, and equity awards. The position can be based in Cincinnati, Dallas, or Denver.

Responsibilities

1. Manage successful execution of global studies.
2. Lead teams effectively in a matrix environment.
3. Perform quality checks on submission documents and site essential documents.
4. Prepare and approve informed consent forms.
5. Serve as sponsor contact for start-up and regulatory submissions.
6. Review regulations to develop solutions to start-up challenges.
7. Contribute to business proposals and presentations.
8. Support the growth of departmental staff, processes, and systems.

Qualifications

1. Bachelor's degree required; advanced degree in Life Sciences preferred.
2. Experience with cardiovascular and metabolic indications is desired.
3. At least 5 years of clinical research experience, preferably in a senior/lead role at a CRO.
4. Project management experience and leadership skills.
5. Strong communication skills.
6. Minimal travel required.