Associate Director, Clinical Trial Management
Associate Director, Clinical Trial Management
Medpace
Madrid or Remote, Spain
Job Summary
Medpace is the leading CRO for Biotech companies and is continuing to add senior-level Project Managers and established Associate Directors to join our Clinical Trial Management Group in Spain. Our therapeutic areas of focus include Oncology, Cardiovascular/Metabolic, Infectious Disease, CNS, Immunology, and more. We provide remote flexibility only with relevant CTM/PM experience. 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;
- 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; required for home-based;
- Management of overall project timeline;
- Bid defense experience, preferred;
- Strong leadership skills.
Don't forget to mention EuroPharmaJobs when applying.
