Associate Director, Clinical Trial Management

Medpace, Inc.•Cincinnati, OH

115d•Hybrid

About The Position

Medpace is seeking to hire established Clinical Trial Managers / Project Managers to join our Clinical Trial Management Group across our US offices. Our therapeutic areas of focus include Oncology/Hematology, Cardiovascular, Renal, Gastrointestinal, Endocrine/Metabolic, Infectious Disease, Neuroscience, and more. We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates.

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
Strong leadership skills

Nice To Haves

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

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