Head of Senior Director, Site Feasibility and Enablement, Americas

BeiGene

8d•$206,200 - $276,200

About The Position

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.

Requirements

Bachelor’s degree (or equivalent) or higher in a scientific, medical or healthcare discipline
minimum of 12 years of combined experience in Feasibility, Clinical Trial Management, Personnel Management and Operations Management.
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, data interpretation to drive inform decision making.
Tried experience in managing, influencing, building, and managing relationships and achieving results with senior partners in conflicting priority environment.
Shown experience or willingness to learn how developing study delivery strategies and tactical/operational plans aligned to commercial and regulatory objectives.
Clinical trial patient and investigator recruitment experience
Validated experience in project and budget management.
Confirmed experience working with Global teams.

Nice To Haves

Microsoft Office Suite, CTMS applications, EDC applications, analytic tools (e.g. Citeline, Trialtrove, etc.) and additional feasibility software

Responsibilities

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.
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
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.
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.
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