Clinical trial management leader overseeing CRO project operations, sponsors, vendors, timelines, and deliverables. Supporting Medpace’s clinical development services for biotech, pharmaceutical, and medical device clients.
Responsibilities
Manage and provide accountability for day-to-day project operations according to the contract, ICH/GCP, and applicable laws and regulations
Serve as the primary Sponsor contact for operational project-specific issues and study deliverables
Maintain in-depth knowledge of the protocol, therapeutic area, and indication
Provide cross-functional oversight of internal project team members and deliverables
Ensure necessary project-specific training is provided
Review and provide input for study protocols, edit check specifications, data analysis plans, and final study reports when applicable
Develop operational project plans
Manage risk assessment and execution
Manage study vendors where applicable
Manage site quality and monitoring deliverables
Requirements
Bachelor’s degree in a health-related field required
Advanced degree in a health-related field preferred
Experience in Phases 1–4; Phases 2–3 preferred
5+ years as a project/clinical trial manager within a CRO required
Experience managing overall project timelines
Bid defense experience
Strong leadership skills
Benefits
Comprehensive health, wellness, retirement, and PTO benefits
Competitive compensation programs that recognize and reward performance
Office-based environment with on-site mentors
Defined career paths with clear advancement opportunities
Industry-renowned onboarding and training programs
Ongoing training and continuous learning opportunities
Company-sponsored social events
Flexible work arrangements: home-based position in Canada; occasional WFH flexibility for eligible positions after training
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