Senior Feasibility and Site Engagement Lead

About us BeOne is a global oncology company that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a broad portfolio, we are expediting development of our diverse pipeline of novel therapeutics through our internal capabilities and collaborations. We are committed to radically improving access to medicines for far more patients who need them. Our growing global team of more than 10,000 colleagues spans five continents, with administrative offices in Basel, Beijing, and Cambridge, U.S. To learn more about BeOne , please visit www.beonemedicines.com and follow us on LinkedIn and X (formerly known as Twitter). 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. Job Description: General Description: The Senior Feasibility and Site Engagement Lead will serve as a value-added resource to sites and investigators and support the Company’s Clinical Development Programs. The Senior Feasibility and Site Engagement Lead will be responsible for building and managing relationships with Key Opinion Leaders (KOLs), clinical trial investigators, and research staff to ensure full engagement throughout an asset’s clinical development. They will also work to build relationships, where appropriate, with scientific organizations and academic organizations. Being regionally based, the primary focus of the Senior Feasibility and Site Engagement Lead role will be to enhance clinical trial protocol designs, feasibility, protocol execution and enrollment through building close relationships with study investigators and research staff in their region. The Senior Feasibility and Site Engagement Lead will work with the clinical investigators and site staff to provide; education, support patient enrollment and retention initiatives identify, mitigate, and provide solutions to enrollment hurdles disseminate investigational product/trial information provide scientific intelligence and represent company interests. The Senior Feasibility and Site Engagement Lead, develops relationships with internal cross functional teams members to ensure the delivery of, high-quality feasibility/site identification assessments. Expertise in the region about Standard of Care, disease landscape and competitive intelligence, including but not limited to competing trials, recent or upcoming approvals, prescribing data, insurance claims data, and recruitment capabilities. This includes conducting feasibility outreach and participating in intelligence gathering and risk assessment to coordinate feasibility projects and deliverables. Aligned with global feasibility and the site management team, this position will play a critical role in data-driven strategic design and operational feasibility, site identification, patient recruitment and retention recommendations for early to late-stage assets development across global clinical operations (GCO) at the concept stage through to execution. Territories for the Senior Feasibility and Site Engagement Lead position will vary as needs arise and develop. Essential Functions of the job: Serves as the primary point of contact for feasibility conducted in the region and liaises cross-functionally to enable expedited, predictive delivery at all stages of regional feasibility Ensures standardization in the use of data, tools, and processes to support quality decision-making at the therapeutic area, disease indication, programs, and study levels during feasibility output In partnership with internal stakeholders, including regional leaders (e.g., country heads, regional study managers) and site management (e.g., CRAs, trial oversight managers) - combines and integrates data to provide clear recommendations for feasibility Strengthens data-driven trend analysis, identifies root causes, and provides relevant recommendations across study teams and programs to accelerate study execution Provides data-driven operational strategy during feasibility analyses, including site identification, patient recruitment and retention recommendations taking into consideration unmet medical needs of the patient population, study, and business priorities. Collects and analyzes all data (e.g., local standard of care treatment, available treatment options approved/reimbursed, local incidence/prevalence of disease, access to the targeted patient population, drug landscape, historical/current clinical trial landscape) to influence and inform protocol development, operational plans, establish a geographic country footprint and proposed sites for participation in a clinical study. Uses all competitive intelligence to develop data-driven study startup forecasts, bench-marking assumptions, and accurate enrollment plans. Develops deep insights, uncovers unmet needs, and collaborates within a global matrix team. Explains data to facilitates data-driven decision-making processes. Partners with study design teams on protocol optimization, enabling data-driven approaches to inform decision-making and improve the predictability of execution Contributes to improvement and implement creative processes, methodologies, data, and technologies to ensure continuous delivery of high quality of feasibility and study startup Leads and contributes to Strategic planning meetings, regional in-depth capabilities meetings, training calls, kick-off meetings and ongoing team meetings to confirm the adequacy of sites/enrollment and ongoing feasibility support. Leverages leading industry tools and data sources to provide data on startup timelines, past recruitment rates and performance (data quality, startup cycle time, query rate, protocol deviations, and inspection results) to assist project teams with study initiation timeline forecasting. In collaboration with internal study team and CRO (if applicable), supports the re-forecasting of patient enrollment models to adjust for new environmental influences (e.g., change in drug landscape, protocol amendment, increased screen failure rate). Determines risks/mitigation for the study feasibility and patient recruitment Maintains current therapeutic area knowledge and assesses the impact of evolving information on operational strategies. Exhibits the ability to perform root cause analysis and determine mitigation steps to removing roadblocks related to study execution and patient enrollment. Participates in regional and global projects representing Clinical Operations and Study Optimization initiatives to support BeOne’s R&D goals. Builds and cultivates relationships with disease area experts (KOLs), Clinical Investigators in the disease area, Research sites, and staff and i