Associate Director, Clinical Trial Management - Canada

Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers / Clinical Project Directors to join our team in Canada. Our therapeutic areas of focus include Oncology/Hematology, Cardiovascular, Renal, Gastrointestinal, Endocrine/Metabolic, Immunology, Inflammation, Infectious Disease, Neuroscience, Ophthalmology and more . This is a home-based position in Canada. 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 required; 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; Management of overall project