Director, Clinical Trial Management

Medpace; Cincinnati (OH); Remote; USD 125,000 - 150,000; Full time

Job summary

A leading clinical research organization is seeking Senior Directors and Project Managers to join their Clinical Trial Management Group in Cincinnati, OH. The role involves managing project operations, serving as the primary contact for sponsors, and leading cross-functional teams. Candidates should have a bachelor's degree in a health-related field, along with 5+ years of project management experience within a CRO. Competitive salary and equity opportunities are offered.

Benefits

Competitive salary/bonus program

Equity grants

Qualifications

• Bachelor’s degree in a health-related field; advanced degree preferred.
• 5+ years as a project/clinical trial manager within a CRO.
• Strong leadership skills and experience managing timelines.

Responsibilities

• Manage day-to-day operations of the project according to contract.
• Serve as primary Sponsor contact for project-specific issues.
• Develop operational project plans.

Job description

Overview

Medpace is the leading CRO for Biotech companies and is continuing to add senior-level Directors and established Project Managers to join our Clinical Trial Management Group in Cincinnati, OH, Dallas, TX, Denver, CO or remotely with relevant experience. Our therapeutic areas of focus include Oncology/Hematology, Cardiovascular/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.

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

Qualifications

• Bachelor’s degree in a health-related field; 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
• Management of overall project timeline
• Bid defense experience
• Strong leadership skills