Senior Associate Director, Clinical Trials Leadership

Medpace; Cincinnati (OH); On-site; USD 110,000 - 150,000; Full time

Benefits offered by this job

Competitive compensation

Health, retirement, PTO benefits

On-site culture with occasional WFH

Company-sponsored social events

Job summary

Medpace, a leading CRO based in Cincinnati, is seeking a Clinical Trial Manager/Project Manager to oversee day-to-day operations across trials in multiple therapeutic areas. You will coordinate cross-functional teams, ensure adherence to ICH/GCP, and serve as sponsor liaison.

Responsibilities include developing project plans, managing timelines, risk assessment, vendor oversight, and maintaining protocol knowledge.

Qualifications

• Bachelor’s degree required; advanced degree preferred.
• 5+ years as a project/clinical trial manager within a CRO.
• Experience in Phases 1-4; Phases 2-3 preferred.
• Management of overall project timeline.
• Bid defense experience preferred.
• Strong leadership skills.

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

Skills

Leadership

Project management

Education

Bachelor’s degree in a health-related field

Advanced degree in a health-related field

Job description

Medpace, a leading CRO based in Cincinnati, is seeking a Clinical Trial Manager/Project Manager to oversee day-to-day operations across trials in multiple therapeutic areas. You will coordinate cross-functional teams, ensure adherence to ICH/GCP, and serve as sponsor liaison.

Responsibilities include developing project plans, managing timelines, risk assessment, vendor oversight, and maintaining protocol knowledge.