Senior Clinical Project Manager
November 21
Description
• Responsible for planning, execution and management of clinical studies. • Leads study team to deliver studies on time. • Oversees CROs ensuring compliance with study plans and regulations. • Monitors clinical trial progress, budget and timelines. • Establishes collaborative relationships with partners.
Requirements
• S./M.S./Ph.D. in a related life science discipline preferred. • Thorough understanding of the oncology arena. • Minimum of 3-5 years of industry experience in clinical drug or program development or equivalent academic experience in clinical trials.
Benefits
• Merit-based salary increases. • Short incentive plan participation. • Eligibility for 401(k) plan. • Medical, dental, vision, life and disability insurances. • Unlimited paid time off. • 11 paid holidays plus additional time off for shutdown in December. • 80 hours of paid sick time upon hire and each year thereafter.
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