Senior Manager, Clinical Project Management

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November 5

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Sumitomo Pharma America, Inc.

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Biotechnology • Pharmaceuticals • Healthcare Insurance

Sumitomo Pharma America, Inc. is dedicated to improving the health and well-being of people around the world by driving innovative treatments, science, and technology. The company focuses on addressing patient needs in critical areas such as psychiatry & neurology, oncology, urology, women's health, rare diseases, and cell & gene therapy. As a subsidiary of Sumitomo Pharma Co. , Ltd. , SMPA embodies the promise of combining technology and life-sciences expertise to improve patient outcomes. With a diverse pipeline of preclinical and clinical programs, SMPA is committed to delivering patient-first solutions through a technology-driven approach.

1001 - 5000 employees

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

📋 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