Global Study Start-Up Project Manager
Location: Remote – United States
Job Category: Site Activation & Maintenance
Job ID: 10828
Job Summary
Medpace, a leading full-service Clinical Research Organization (CRO), is seeking an experienced Global Study Start-Up Project Manager to join our rapidly growing Clinical Operations team. This role is critical in accelerating clinical trial initiation and ensuring regulatory and operational compliance across global study sites.
This position offers remote work flexibility with performance-based incentives, including competitive bonuses, sign-on/relocation bonuses, and equity awards for eligible candidates.
Key Responsibilities
Lead global study start-up, maintenance, and close-out activities to ensure timely execution and regulatory compliance
Serve as the primary Sponsor contact for start-up and regulatory submission activities
Perform quality checks on submission documents and site essential documentation
Prepare, review, and approve Informed Consent Forms and other study documentation
Conduct regulatory reviews to develop proactive solutions for study start-up challenges
Prepare new business proposals and contribute to bid defenses, general capabilities meetings, and audits
Provide mentorship and development to departmental staff, supporting process improvements and system enhancements
Collaborate across matrix teams to ensure project deliverables align with study timelines and quality standards
Required Experience & Qualifications
Bachelor’s degree in Life Sciences or a related field; Advanced degree preferred
5+ years of clinical research experience, ideally in a senior or lead Study Start-Up role within a CRO
Demonstrated project management skills and ability to develop and mentor team members
Strong oral and written communication skills
Minimal travel required
Why Medpace?
Medpace is a globally recognized mid-sized CRO delivering Phase I–IV clinical development services across biotechnology, pharmaceutical, and medical device industries. Our disciplined and scientific approach accelerates the global development of safe and effective therapeutics, leveraging local regulatory and therapeutic expertise across multiple therapeutic areas, including oncology, cardiology, metabolic disease, endocrinology, CNS, anti-viral, and anti-infective.
Headquartered in Cincinnati, Ohio, with over 5,000 employees in 40+ countries
Strong focus on employee career growth, training, and development
Perks & Benefits
Flexible, remote-friendly work environment
Competitive PTO packages, starting at 20+ days
Comprehensive compensation and benefits package
Company-sponsored employee appreciation events
Employee health and wellness programs
Structured career growth and professional development paths
Local discounts for shopping, fitness, and entertainment
Awards & Recognition
Named a Top Workplace in 2024 by The Cincinnati Enquirer
Recognized by Forbes as one of America’s Most Successful Midsize Companies (2021–2024)
Recipient of CRO Leadership Awards from Life Science Leader magazine for expertise, quality, and reliability
Next Steps
Qualified candidates will be reviewed by the Medpace recruitment team. Shortlisted applicants will be contacted with next steps for the selection process.
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