Senior Manager, Clinical Project Management

Job Description: • Represents and leads the study team to design, develop and deliver the clinical study to agree upon timelines • Leads planning and communication with cross-functional teams to ensure proper execution and conduct of the clinical trial • Serves as primary contact and resource for CRO and vendor personnel in overarching functions • Provides oversight and management of CROs, consultants and vendors • Monitors progress of clinical activity and reports on the progress of assigned clinical trials including budget and timelines • Prepares potential investigator site lists and assists with their evaluation for inclusion in the study • Participates in meetings – i.e. Study Team Meetings, Investigator Meetings, Monitors’ workshops and CRO Training Requirements: • Bachelor’s degree in a related field required • M.S./Ph.D. in a related life science discipline is preferred • Minimum of 3-5 years of industry experience in clinical drug or program development or equivalent academic experience in clinical trials • Strong experience facilitating project team meetings, cross-functional communication and decision making • Familiarity with the design and conduct of clinical trials and project management in relevant therapeutic areas • Strong analytical skills with a data driven approach to planning, executing, and problem solving • Working knowledge of current global regulatory requirements and guidelines for clinical trials Benefits: • merit-based salary increases • short incentive plan participation • eligibility for our 401(k) plan • medical, dental, vision, life and disability insurances • flexible paid time off • 11 paid holidays plus additional time off for a shut-down period during the last week of December • 80 hours of paid sick time upon hire and each year thereafter Apply tot his job