Senior Manager, Clinical Trial Analytics
Location: Princeton, NJ, US | Madison - Giralda, NJ, US
About Bristol Myers Squibb
At Bristol Myers Squibb, we transform patients' lives through science. Our work is meaningful, challenging, and life-changing. From optimizing production lines to breakthroughs in cell therapy, every department contributes to this mission. You'll have opportunities to grow, thrive, and make a lasting impact alongside a diverse and high-achieving team.
BMS values work-life balance and flexibility, offering competitive benefits, services, and programs to support employees in both their professional and personal lives. Learn more: careers.bms.com.
Position Summary
The Senior Manager, Global Feasibility is a highly skilled clinical research professional responsible for analyzing clinical trial intelligence data to drive study feasibility assessments, country and site selection, and data-driven patient recruitment and enrollment forecasts for clinical trials across all phases.
Key Responsibilities
Clinical Development Strategy: Provide input into clinical development plans for indications and programs, including country and site tiering.
Feasibility & Site Selection: Lead feasibility assessments for Phase I-III clinical trials by analyzing disease prevalence, treatment landscapes, and competitive intelligence.
Country & Site Evaluation: Collect and assess data on local treatment standards, available therapies, and patient access to define optimal site selection.
Study Execution: Conduct feasibility assessments, evaluate site performance, and execute data-driven country and site selection.
Patient Enrollment Forecasting: Build and maintain study-level and country-level patient enrollment models, considering site activation rollout and external variables.
Scenario Modeling: Re-project and re-plan accrual forecasts, identifying and mitigating potential risks to study timelines.
Ongoing Study Oversight: Track and analyze patient enrollment trends, updating teams on performance and identifying necessary adjustments.
Cross-Functional Collaboration: Work closely with study teams, country site selection teams (CSST), and other key stakeholders to ensure smooth trial execution.
Advanced Data Analysis: Provide ad-hoc insights and analytics to support governance and operational decision-making.
Process Optimization: Contribute to initiatives aimed at enhancing study planning, execution, and efficiency.
Qualifications & Experience
Education: Bachelor’s degree in Life Sciences, Epidemiology, Information Science, or related field (Advanced degree preferred).
Experience:
3+ years in clinical research, pharmaceutical, or healthcare industry.
Experience with country and site selection, trial feasibility, and enrollment forecasting preferred.
Strong background in data analysis and industry intelligence tools.
Key Competencies:
Advanced proficiency in Microsoft Excel (formulas, graphs, pivot tables).
Strong analytical and problem-solving skills.
Effective communication and collaboration across cross-functional teams.
Ability to manage multiple projects with minimal oversight.
Strong leadership and decision-making abilities.
Why Join Us?
At BMS, every employee plays a critical role in shaping the future of healthcare. Our commitment to passion, innovation, urgency, accountability, inclusion, and integrity creates an environment where diverse talents thrive. If this opportunity excites you, but you don’t meet every qualification, we encourage you to apply—you may be one step away from transforming your career and making a difference in patients’ lives.
Apply now and be part of something bigger.
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