Sumitomo Pharma America, Inc.
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.
Medical Director, Clinical Research
Job not on LinkedIn
November 15
Sumitomo Pharma America, Inc.
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.
📋 Description
• Lead and demonstrate ownership of the design and implementation of a clinical development program • Oversee project-related education of investigators, study site personnel, and study staff • Responsible for leading clinical study teams and monitoring overall study integrity • Present at scientific, medical, and regulatory meetings globally • Develop and maintain relationships with academic investigators, pharmaceutical partners/sponsors, and patient advocacy groups • Contribute to company’s planned regulatory filings including authoring clinical sections for INDs, NDAs, and related documents
🎯 Requirements
• Medical Doctor (MD), Doctor of Osteopathy (DO), or non-US equivalent of MD required • Completion of a residency program strongly preferred • Completion of a subspecialty fellowship is desirable • Experience in blood cancers or solid tumors desirable • At least 3 years of pharmaceutical drug development experience required
🏖️ Benefits
• Health insurance • 401(k) plan • Flexible paid time off • 11 paid holidays • Additional time off during shut-down period in December • 80 hours of paid sick time upon hire and each year thereafter
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