
Job Overview
Location
Remote (US)
Job Type
Full-time
Category
Data Science
Date Posted
June 14, 2026
Full Job Description
📋 Description
- • Lead the development and execution of a regional site feasibility and engagement strategy across the Americas to support the global clinical development portfolio.
- • Oversee country and site feasibility assessments using data analytics, historical trial performance, competitive intelligence, disease prevalence, and local treatment standards to drive evidence-based site selection.
- • Standardize and continuously improve feasibility processes, tools, and governance frameworks to enhance efficiency and accuracy in clinical trial startup.
- • Design and implement strategic site engagement models that foster long-term partnerships with investigative sites, site networks, and key opinion leaders (KOLs).
- • Expand clinical trial access to underserved communities through culturally aligned, locally relevant engagement strategies in collaboration with regional teams.
- • Develop accurate enrollment forecasts and study startup timelines using competitive intelligence, adjusting for emerging factors and implementing risk mitigation plans.
- • Lead the design and execution of study-specific patient recruitment programs in partnership with study teams, CROs, and vendors to optimize participant enrollment and retention.
- • Implement innovative technologies, methodologies, and data-driven tools to enhance feasibility, site activation, and recruitment outcomes.
- • Conduct root cause analysis of enrollment and trial execution challenges and develop actionable mitigation strategies to improve trial performance.
- • Manage and lead cross-functional teams including Country Feasibility, Clinical Trial Diversity, Site Partnerships, and Patient Recruitment and Retention functions.
- • Drive cross-functional governance to align site selection, activation, and enrollment execution across clinical operations and global stakeholders.
- • Stay current with therapeutic area advancements and assess their impact on operational feasibility and trial design strategies.
- • Contribute to strategic planning, capability assessments, and training initiatives to strengthen the organization’s feasibility and enablement capabilities.
- • Collaborate with global teams to support BeOne R&D goals and represent Clinical Operations in regional and global projects.
- • Utilize Microsoft Office Suite, CTMS, EDC, and specialized feasibility software (e.g., Citeline, Trialtrove) to analyze data and support decision-making.
- • Manage project timelines, budgets, and resources with proven expertise in clinical trial operations and site enablement.
- • Apply analytical thinking and data interpretation to inform strategic decisions and drive operational excellence in clinical trial execution.
- • Demonstrate strong communication, influence, and relationship-building skills with senior partners in high-priority, conflicting-environment settings.
- • Travel may be required based on business needs.
Skills & Technologies
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About BeiGene, Ltd.
BeiGene is a global biotechnology company discovering, developing, manufacturing and commercializing innovative oncology medicines. Its broad pipeline includes more than 50 clinical-stage molecules, spanning targeted therapy, immuno-oncology and combination regimens. Core products are BTK inhibitor BRUKINSA, PD-1 antibody tislelizumab and PARP inhibitor pamiparib, marketed worldwide through internal teams and strategic alliances. BeiGene operates integrated research campuses in Beijing and Cambridge, MA, a manufacturing facility in Suzhou and offices across North America, Europe and Asia-Pacific, serving patients in more than 45 countries.
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