Director, Clinical Trial Management

Medpace, Inc.•Cincinnati, OH

116d•Hybrid

About The Position

Medpace is seeking to add senior-level Directors and established Project Managers to join our Clinical Trial Management Group. This role involves managing and providing accountability for the day-to-day operations of clinical trials, serving as the primary Sponsor contact, and ensuring adherence to ICH/GCP and other applicable regulations. The position requires maintaining in-depth knowledge of protocols and therapeutic areas, providing cross-functional oversight, and developing operational project plans. Responsibilities also include risk management, vendor management, and site quality oversight.

Requirements

Bachelor’s degree in a health-related field
Experience in Phases 1-4
5+ years as a project/clinical trial manager within a CRO
Management of overall project timeline
Bid defense experience
Strong leadership skills

Nice To Haves

Advanced degree in a health-related field
Phases 2-3 preferred

Responsibilities

Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations
Serve as primary Sponsor contact for operational project-specific issues and study deliverables
Maintain in depth knowledge of protocol, therapeutic area, and indication
Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided
Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable
Develop operational project plans
Manage risk assessment and execution
Manage study vendors where applicable
Manage site quality and monitoring deliverables