Senior Director, Head of Site Feasibility and Enablement, Americas

๐Ÿข BeiGene ยท all BeiGene jobs
๐Ÿ“ United States
๐Ÿ’ฐ USD 206,200 - 276,200 / annual
๐Ÿ“… Posted 2026-07-03 ยท via Himalayas
๐Ÿท Site-Feasibility,Clinical-Operations,Site-Partnerships,Patient-Recruitment,Clinical-Development-Leadership,Director-Of-Field-Enablement-and-Organizational-Design,Director-of-Global-Enablement,Director-Clinical-Site-Operations,Associate-Director-Site-Oversight
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BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.
General Description:

As the Head of Site Feasibility and Enablement, Americas within Global Clinical Operations (GCO), you will hold a strategic leadership role responsible for defining and executing the site feasibility and engagement strategy across the clinical development portfolio in the Americas. This role ensures accurate enrollment planning, optimal site selection, increased clinical trial access, and acceleration in activation and enrollment through site partnerships, patient recruitment strategies, and innovative enablement approaches. This position plays a critical role in shaping how the organization identifies, evaluates, and supports investigative sites, while continuously assessing the external landscape for tools, technologies, and recruitment trends to enhance trial execution.
Essential Functions of the job:

Feasibility Strategy and Execution :

- Develop and lead a regional feasibility strategy aligned with portfolio priorities and timelines

- Oversee country and site feasibility assessments, integrating data analytics, historical performance, and competitive intelligence

- Ensure feasibility outputs drive robust, evidence-based site selection decisions

- Standardize and continuously improve feasibility processes, tools, and governance

- Utilize comprehensive data analysis, including local treatment standard of care, disease prevalence, drug landscape, and historical trial data, to inform protocol development and establish geographic footprints and proposed sites for participation in clinical studies.

Site Engagement and Partnerships:

- Establish and maintain strategic relationships with key investigative sites, site networks, and KOLs

- Design and implement site engagement models that develop long-term partnerships with key investigative sites

- Lead efforts to expand clinical trial reach to underserved communities

- Partner with countries in assigned region to ensure culturally aligned and locally relevant engagement strategies

Enrollment Forecasting and Risk Mitigation:
- Utilize competitive intelligence data to develop accurate study startup forecasts, benchmark assumptions, and enrollment plans.

- Maintain patient enrollment forecasts strategically, adjusting for new influencing factors and developing risk mitigation plans.

- Lead the design and implementation of study-specific recruitment programs, collaborating with study teams, vendors, and CROs as needed to optimize participant recruitment.

Continuous Improvement and Innovation:
- Implement creative processes, methodologies, data, and technologies to enhance the delivery of Feasibility, Study Startup Services, and recruitment and retention strategies

- Contribute to ongoing strategic planning, capability assessments, and training efforts to ensure successful feasibility support.

- Stay up to date with current therapeutic area knowledge, assessing its impact on operational strategies.

- Perform root cause analysis and develop mitigation strategies to address study execution and enrollment challenges.

- Participate in regional and global projects, representing Clinical Operations to support BeOne R&D goals.

Supervisory Responsibilities:

- Drive cross-functional governance to support site selection, activation, and enrollment execution

- Line Manage - Country Feasibility, Clinical Trial Diversity, Site Partnerships, and Patient Recruitment and Retention teams

Computer Skills: Microsoft Office Suite, CTMS applications, EDC applications, analytic tools (e.g. Citeline, Trialtrove, etc.) and additional feasibility software
Other Qualifications:
- Experience with trial optimization vendors, tools, and me

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