Clinical Trial Manager Associate, Clinical Operations

🕒 July 24

🇺🇸 United States – Remote

💵 $107.5k - $130.3k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🏥 Clinical Operations

🚫👨‍🎓 No degree required

🦅 H1B Visa Sponsor

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Logo of Bristol Myers Squibb

Bristol Myers Squibb

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 RayzeBio SOPs, FDA regulations, and ICH/GCP guidelines • Participate in vendor meetings • Develop and manage vendor study operational plans and risk mitigation strategies • Review key performance indices and vendor metrics • Assist the Study Lead with management of the study CRO • Review the Clinical Study Protocol, Informed Consent Forms, and other study documents and plans • Participate in CRO and Study Execution Team meetings • Provide input to operational strategy, including study and country start-up • Support site feasibility, selection, initiation, and issue resolution • Track and maintain study documentation, including TMF 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 • Independent professional who proactively communicates frequently and effectively • 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 • Expertise in Microsoft Project and Smartsheets desired • Up to 10% travel required

🏖️ Benefits

• Discretionary incentive cash • Stock opportunities • Wellbeing support • Retirement and financial protection benefits • Medical, dental, vision, life and disability insurance offerings • Flexible Time Off (FTO) without a set accrual limit for eligible U.S.-based exempt employees • 11 paid company holidays each year • 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, depending on eligibility • Up to two paid volunteer days per year • Summer hours flexibility • Leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs • Annual Global Shutdown between Christmas Day and New Year's Day for eligible employees • Reasonable workplace accommodations/adjustments and ongoing support

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