Overview
In this role you drive the day-to-day delivery of clinical trial operations in London within Medpace’s Clinical Trial Management Group. You leverage your therapeutic expertise (Cardiovascular/Endocrine/Metabolic) while ensuring compliance with ICH/GCP and applicable laws. You partner with sponsors and cross-functional teams to manage timelines, risks, vendors, and study deliverables, shaping trial execution at a leading CRO. This is a hands-on role with meaningful impact on trial success and patient outcomes.
Pay / Benefits
- Flexible work environment
- Competitive compensation and benefits package
- Competitive PTO packages
- Structured career paths with opportunities for professional growth
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
Responsibilities
- Manage day-to-day operations of trials per contract, ICH/GCP standards and regulations
- Serve as primary Sponsor contact for operational issues and deliverables
- Maintain in-depth knowledge of protocol, therapeutic area, and indication
- Provide cross-functional oversight and ensure project-specific training for team members
- Review input for study protocol, edit check specs, data analysis plan, and final study report
- Develop operational project plans and manage risk assessment and execution
- Oversee study vendors and monitor site quality; supervise CRAs and deliverables
Key requirements
- Bachelor’s degree in health or life sciences; advanced degree preferred
- 5+ years of Clinical Trial Management experience; CRO experience preferred
- Experience in Phases 1-4 (Phases 2-3 preferred)
- Experience managing overall project timelines; bid defense experience preferred
- Strong leadership and stakeholder management skills
- Leadership
- Cross-functional collaboration
- Effective communication with sponsors and teams
- ICH/GCP compliance
- Protocol review and study design input
- Data analysis plan and final study report knowledge
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