Senior Clinical Trial Manager, Associate Clinical Operations

🕒 July 6

🇺🇸 United States – Remote

💵 $119.1k - $144.3k / year

⏰ Full Time

🟠 Senior

🏥 Clinical Operations

🦅 H1B Visa Sponsor

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👻 Ghost score 34%

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Bristol Myers Squibb

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1887

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

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.

📋 Description

• Manage study vendors including Central Lab, RTSM/IRT, Imaging, and Dosimetry Vendors • Ensure vendor deliverables are on time, within budget, and compliant with SOPs, FDA regulations, and ICH/GCP guidelines • Participate in vendor meetings and manage vendor operational plans and risk mitigation strategies • Review vendor performance indices and metrics • Assist the Study Lead with CRO management and review clinical study protocols, informed consent forms, study documents, and plans • Participate in CRO and Study Execution Team meetings and contribute to operational strategy, study, and country start-up • Support site feasibility, selection, initiation, and issue resolution • Track and maintain study documentation, including Trial Master File completeness and quality • Monitor and report vendor progress and escalate issues to internal stakeholders • Assist with study vendor budgets and invoicing according to study contracts • Summarize vendor performance data and escalate study risks to the Study Lead • Use AI tools to enhance individual productivity and quality of work

🎯 Requirements

• Minimum 2-3 years clinical operations experience within biotech, pharma or CRO industry • BA/BS degree in a scientific or healthcare discipline preferred • Expertise in Microsoft Project and Smartsheets desired • Proactive and frequent communication • Detail and action-oriented, organized, and committed to quality and consistency • Ability to work successfully in cross-functional teams • Ability to work in a dynamic environment with a high degree of flexibility • Up to 10% travel required

🏖️ Benefits

• Additional discretionary incentive cash and stock opportunities • Wellbeing support benefits • Retirement and financial protection benefits • Medical, dental, vision, life and disability insurance offerings • Flexible Time Off (FTO) for U.S.-based exempt employees • 11 paid company holidays • 160 hours of paid vacation annually for new hires for non-exempt employees, RayzeBio employees, and employees located in Puerto Rico • 3 optional holidays for non-exempt employees, RayzeBio employees, and employees located in Puerto Rico • Paid sick leave, subject to eligibility • Up to two paid volunteer days per year • Summer hours flexibility • Medical, personal, parental, caregiver, bereavement, or military leaves of absence • Annual Global Shutdown between Christmas Day and New Year's Day