Job SummaryMedpace is the leading CRO for Biotech companies and is continuing to add established
Clinical Trial Managers and Project Managers with a focus on
Oncology/Hematology to join our Clinical Trial Management Group in our Cincinnati, OH office. 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;
- Responsible for management of study vendor; and
- Manage site quality, including direct supervision of project Clinical Research Associates 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; and
- Strong leadership skills.
What to Expect NextA Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
