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Senior Director, Head of Feasibility, Americas

BeOne Medicines
Full-time
Remote friendly (United States)
United States
$202,200 - $272,200 USD yearly
Clinical Research and Development

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Role Summary

Senior Director, Head of Feasibility, Americas. BeOne seeks a highly motivated, collaborative leader to deliver data-driven feasibility reports for early to late-stage medicines development, overseeing site identification and recruitment/retention recommendations to support clinical trial execution.

Responsibilities

  • Act as the primary point of contact for Global Strategic Feasibility and Regional Clinical Operations teams for Feasibility and Re-Feasibility activities.
  • Liaise cross-functionally to deliver feasibility insights at various levels (TA, indication, program, study), ensuring standardization of data, tools, and processes for quality decision-making.
  • Combine and integrate data from internal and external sources to provide clear feasibility strategies for site identification, recruitment, and retention at the TA/indication/program level.
  • Utilize data analysis to inform protocol development and establish geographic footprints and proposed sites for participation in studies.
  • Consider the unique needs of each indication, patient population, study, and business priorities.
  • Develop accurate study startup forecasts, benchmark assumptions, and enrollment plans using competitive intelligence data.
  • Maintain patient enrollment forecasts and develop risk mitigation plans; design and implement study-specific recruitment programs in collaboration with study teams, vendors, and CROs.
  • Implement processes, methodologies, data, and technologies to enhance feasibility and study startup services; contribute to strategic planning and training.
  • Stay current with therapeutic area knowledge and assess its impact on operational strategies; perform root cause analysis and mitigation strategies for study execution and enrollment challenges.
  • Participate in regional/global projects representing Clinical Operations and Study Optimization to support R&D goals.
  • Lead and nurture ownership and accountability within the team and with external stakeholders; line manage Country Feasibility and Clinical Trial Diversity teams.

Qualifications

  • Experience with trial optimization vendors, tools, and methods; proficiency with software models and database structures.
  • Expertise in principles driving country/site identification, feasibility, and study startup strategies.
  • Validated experience in data analysis and data interpretation to drive informed decision making.
  • Experience managing and influencing senior partners in conflicting priority environments.
  • Ability to develop study delivery strategies and tactical/operational plans aligned to commercial and regulatory objectives.
  • Clinical trial patient and investigator recruitment experience; project and budget management experience.
  • Experience working with Global teams.
  • Travel may be required as per business need.

Education

  • Bachelorβ€šΓ„Γ΄s degree (or equivalent) or higher in a scientific, medical, or healthcare discipline with a minimum of 12 years of combined experience in Feasibility, Clinical Trial Management, Personnel Management, and Operations Management.

Skills

  • Strategic liaison and cross-functional coordination
  • Data-driven feasibility planning and site identification
  • Enrollment forecasting and risk mitigation
  • Continuous improvement and innovation in feasibility and study startup services
  • Strong analytical thinking and data analysis
  • Effective communication with clarity and stakeholder management

Additional Requirements

  • Experience with Global teams and leading regional feasibility initiatives.
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