Clinical Trial Manager, Clinical Operations

🔥 0 minutes ago

🇺🇸 United States – Remote

💵 $107.5k - $130.3k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🏥 Clinical Operations

🚫👨‍🎓 No degree required

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 0%

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.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

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 • Develop and manage risk mitigation strategies • Review key performance indices and vendor metrics • Assist the Study Lead with CRO management and review 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 Trial Master File completeness and quality • Monitor and report vendor progress and escalate issues to internal stakeholders • Assist with study vendor budgets and invoicing procedures • 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 • Ability to proactively communicate 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 • Up to 10% travel required

🏖️ Benefits

• Additional discretionary incentive cash and 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 • Paid sick leave • 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