Clinical Trials Manager, Clinical Operations

🕒 July 27

🇺🇸 United States – Remote

💵 $134.5k - $163k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

🏥 Clinical Operations

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 43%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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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

• Lead the planning, execution, and closeout of Phase I–III clinical trials • Oversee and manage CROs and vendors to ensure timely, on-budget, compliant study completion • Lead the cross-functional study execution team in achieving study goals and deliverables • Plan and execute study timelines • Monitor enrollment, site performance, data quality, and key risk indicators • Proactively escalate issues to internal stakeholders for timely resolution • Identify, assess, and mitigate operational risks • Manage study CRO and vendor budgets and invoicing procedures according to study contracts • Lead or support country and site feasibility, selection, and activation strategies • Participate in CRO and vendor meetings • Review CRO and vendor operational plans and provide input to operational strategy • Summarize CRO, vendor, and site performance data and escalate study risks to the Clinical Operations Program Lead / Head of Clinical Operations • Perform other related duties as assigned

🎯 Requirements

• Minimum 5–7 years clinical operations experience within biotech, pharma or CRO industry • BA/BS degree in a scientific or healthcare discipline preferred • 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 • Applies AI to improve team execution and decision-making • Compliance with corporate and program SOPs, GCP/ICH guidelines, and applicable FDA and state regulations • Up to 20% travel required

🏖️ Benefits

• Wellbeing support • 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 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 • Reasonable workplace accommodations/adjustments and ongoing support for people with disabilities