Associate Director - Cell Therapy Clinical Product Administration Process Excellence

2 days ago

🏄 California – Remote

Although this job is listed in California, this company may be open to hiring remote in other states.

🌽 Illinois – Remote

Although this job is listed in Illinois, this company may be open to hiring remote in other states.

+3 more states

🏄 California – Remote 🌽 Illinois – Remote 🏖️ New Jersey – Remote 🍂 Massachusetts – Remote 🤠 Texas – Remote

💵 $156k - $195k / year

⏰ Full Time

🟠 Senior

😶‍🌫️ Therapist

🦅 H1B Visa Sponsor

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Bristol Myers Squibb

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Bristol Myers Squibb is a global biopharmaceutical company that is dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. Their areas of focus include cardiovascular health, cell therapy, immunology, and oncology. With a commitment to transforming patient outcomes through pioneering science, Bristol Myers Squibb partners with a worldwide network of researchers, healthcare providers, and other stakeholders. They aim to lead in innovation for patients while fostering diversity and inclusion within their workforce.

biotechnology • innovation • great place to work • pharmaceuticals • research and development

10,000+ employees

Founded 1887

🧬 Biotechnology

💊 Pharmaceuticals

📋 Description

• Associate Director, Cell Therapy Clinical Product Administration Processes (C-PAP) is a key member of the Cell Therapy Franchise Organization. • Provide subject matter expertise (SME) to key internal stakeholders on clinical trial product handling and administration across all phases of Cell Therapy clinical trials. • Collaborate with cross functional partners on process improvement as it relates to Cell Therapy clinical trial execution. • Train and support key study team members on how to execute clinical trial product handling and administration site training. • Author and manage product specific manuals and documents required for the safe execution of clinical trial product handling and administration.

🎯 Requirements

• 6-8 years of relevant experience in clinical research and development or equivalent preferred. • Prior pharmaceutical industry experience which includes experience partnering with Investigators and internal cross functional teams across the matrix preferred (e.g., clinical research scientist, keys study team members, Patients Operations, Manufacturing, etc.). • Excellent communication skills (written and verbal) with the ability to successfully communicate and explain highly technical information in a way that is understandable and usable. • Working knowledge of Hematology, Oncology, Autologous and Allogeneic transplant preferred. • Strong knowledge of clinical trial design, principles, and drug development. • Advanced / independent problem-solving skills. • Proficient in Microsoft Word, Excel, PowerPoint.

🏖️ Benefits

• Medical, pharmacy, dental and vision care. • Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). • Financial well-being resources and a 401(K). • Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. • Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year’s holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. • Parental, caregiver, bereavement, and military leave. • Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. • Other perks like tuition reimbursement and a recognition program.