Study Start-Up Project Manager-Remote

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

Job summary

An established industry player is seeking a Global Study Start-Up Project Manager to enhance their clinical operations team. This role is pivotal in overseeing clinical trial processes, ensuring successful execution of studies, and leading teams in a dynamic environment. With a strong emphasis on project management and leadership, this position offers the opportunity to make strategic decisions that directly contribute to the company's growth. Join a forward-thinking organization that values people and purpose, and be part of a team that has positively impacted countless lives over the years.

Benefits

Flexible work environment

Generous PTO starting at 20+ days

Employee appreciation events

Health and wellness initiatives

Career growth opportunities

Local business discounts

Qualifications

• 5+ years in clinical research, preferably in a senior/lead role.
• Strong project management and leadership skills required.

Responsibilities

• Manage global start-up, maintenance, and close-out studies.
• Lead teams effectively in a matrix environment.
• Prepare and present new business proposals.

Skills

Project Management

Clinical Research

Leadership

Communication Skills

Education

Bachelor's Degree

Advanced Degree in Life Sciences

Job description

Study Start-Up Project Manager - Remote

Job Locations: United States

Job Summary

Are you interested in working in a fast-paced environment where you can make strategic decisions and contribute to a growing and profitable company? Join Medpace! We are expanding our clinical operations and seeking a Global Study Start-Up Project Manager to join our Clinical Operations team. This role is crucial in managing clinical trial processes.

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

Location: Remote

Responsibilities

1. Manage successful execution of global start-up, maintenance, and close-out studies.
2. Lead teams effectively in a matrix environment.
3. Perform quality checks on submission and essential documents.
4. Prepare and approve informed consent forms.
5. Serve as a Sponsor contact for start-up and regulatory submissions.
6. Review regulations to develop proactive solutions to start-up challenges.
7. Prepare and present new business proposals during bid defenses, meetings, and audits.
8. Contribute to the growth and development of staff, processes, and systems.

Qualifications

1. Bachelor's degree required; advanced degree in Life Sciences preferred.
2. 5+ years in clinical research, preferably in a senior/lead role at a CRO in Study Start-Up.
3. Project management experience and leadership skills.
4. Strong communication skills.

Travel: Minimal

Medpace Overview

Medpace is a full-service clinical CRO providing Phase I-IV services to biotech, pharma, and medical device industries. Headquartered in Cincinnati, Ohio, with over 5,000 employees across 40+ countries.

Why Medpace?

We value People, Purpose, and Passion. Our work over 30+ years has positively impacted countless lives. Join us to make a difference.

• Flexible work environment
• Generous PTO starting at 20+ days
• Employee appreciation events
• Health and wellness initiatives
• Competitive pay and benefits
• Career growth opportunities
• Local business discounts

Awards

• Top Workplace 2024 by The Cincinnati Enquirer
• Forbes America's Most Successful Midsize Companies 2021-2024
• CRO Leadership Awards from Life Science Leader magazine

Next Steps

A team member will review your application and contact you if your qualifications match our needs.

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