
10,000+ employees
Founded 1887
🧬 Biotechnology
💊 Pharmaceuticals
Biotechnology • Pharmaceuticals
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.
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10,000+ employees
Founded 1887
🧬 Biotechnology
💊 Pharmaceuticals
Biotechnology • Pharmaceuticals
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.
• Work closely with the study execution team to provide project system, tracking and administrative support in executing all of RayzeBio clinical studies from study start-up, conduct and close-out phases. • Maintain and manage the study Trial Master File (TMF) in compliance with ICH-GCP and company SOPs. • Maintain study team SharePoint sites, study trackers and other databases, which may include data entry and filing of electronic documents. • Track and manage study and site essential documents. • Support vendor and site contract tracking and maintain contracts in applicable RayzeBio systems. • Support organization and management of the study execution team meetings, including meeting coordination, agenda preparation and minutes. • Communicate effectively with all internal and external stakeholders in a positive and professional manner. • Participate in internal audits and inspection readiness activities. • Participate in teleconference calls and meetings as requested.
• Minimum 1-2 years clinical trial experience • Bachelor’s degree required. Life sciences or related field is preferred. • Independent professional who proactively communicates frequently and effectively. • Organized and able to work to on multiple projects with tight deadlines. • High energy level; positive attitude; works well under stress; assertive and effective communicator. • Hands-on, action-oriented, and able to implement effectively. • Uses AI tools to enhance individual productivity and quality of work.
• Health Coverage: Medical, pharmacy, dental, and vision care. • Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP). • Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support. • Work-life benefits include: Paid Time Off US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees). • Paid Time Off Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays.
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