Study Start-Up Project Manager

Medpace; United States; Remote; USD 80,000 - 130,000; Full time

Job summary

A leading clinical research organization is seeking a full-time Global Study Start-Up Project Manager to join their rapidly growing Clinical Operations team. The role involves managing clinical trial studies and contributing strategically to the company's operations. Competitive salary and benefits include bonuses and flexible work arrangements.

Benefits

Flexible work environment

Competitive PTO packages – starting at 20+ days

Company-sponsored employee appreciation events

Employee health and wellness initiatives

Competitive compensation and benefits package

Structured career paths with opportunities for professional growth

Discounts for local businesses

Qualifications

• 5+ years of clinical research experience, preferably in a Senior/Lead role at a CRO.
• Strong oral and written communication skills required.
• Demonstrated role in developing others.

Responsibilities

• Manage global start-up, maintenance, and close-out of studies.
• Lead a matrix environment and serve as a Sponsor contact.
• Prepare and sponsor business proposals.

Skills

Project management

Communication

Leadership

Education

Bachelor's degree

Advanced degree in Life Sciences

Job description

Job Summary

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 inthe clinical trial managementprocess at Medpace.

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

Location: Position is remote.

Responsibilities

• 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.

Qualifications

• Bachelor's degree required, advanced degree in Life Sciences preferred
• 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

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks

• Flexible work environment
• Competitive PTO packages – starting at 20+ days
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives
• Competitive compensation and benefits package
• Structured career paths with opportunities for professional growth
• Discounts for local businesses

Awards

• Named a Top Workplace in 2024 by The Cincinnati Enquirer

• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.