[Remote] Director, GCO Clinical Program Lead (GCPL) – Early Phase

Note: The job is a remote job and is open to candidates in USA. BeOne Medicines is a rapidly growing company focused on fighting cancer, seeking a Director, GCO Clinical Program Lead for Early Phase programs. This role involves strategic operational planning, leadership of global teams, and collaboration across various functions to ensure program success and execution excellence.ResponsibilitiesAccountable and responsible for building, developing and retaining the global team of gCSM, including hiring, training, mentoring, developing direct and indirect reports, performance appraisals and resource managementOversee the delivery and goal achievement of projects within the designated program(s), serving as the point of escalation for resolving issues that gCSM cannot resolveCollaborate with the other GCPLs and Franchise Heads (FH) to define and implement strategies and key priorities across-programs, and establish global standards for goals, performance measures, and capability development for the gCSM rolesGCO Representative for the designated Early Phase program(s)In coordination with Franchise Head, Accountable to the Franchise ERC, DCT and other governance teams as appropriate as GCO representative, to provide clinical operational insight to drive the program strategy and ensure excellence in executionLead/participate in the KOL engagement activities in the designated programs and may act as function spokesperson if neededEvaluate and develop strategic feasibility and budget estimates during Early Planning for new CDPs and upon strategy change during the conduct of a study, where neededAccountable for resource allocation and initiating CST formation; ensures appropriate transition of outputs from early planning to the gCSMCreate and be accountable for the annual program budget and resource forecasts, as well as contributing to and tracking the relevant DCT goals for the programCreate, review, and provide input to and maintain compound-level documents such as IB, DSUR, and protocolOversee timely, quality, and efficient study planning and execution of associated studies within the allocated programConduct regular program review meetings to mentor, support, and ensure all studies are tracking to the DCT/DRC-approved budget and timelineReport on study status, goals, and operational KPIs, and enforce quality KPIs with support from the Compliance teamCollaborate with other GCPLs to evaluate and designate preferred global vendors and participate in vendor governance meetingsCreate or review performance and development plans for direct reports, facilitate and support delivery of performance and development goalsProvide line management and mentorship to gCSMs working within the designated program(s)Inspire and lead efforts to deepen scientific knowledge within the Clinical Operations’ functionChampions a global mindset and approach across Clinical Operations to foster collaboration and consistency across the organizationProvide expert knowledge on the execution of clinical trials through a deep understanding of ICH/GCP Guidelines and other applicable regulatory requirementsPoint of escalation for all compound-related issuesIdentify and drive process improvement initiatives in collaboration with Franchise Head and/or other GCPLs within programCollaborates with cross-functional leaders to provide operational perspectives to enable effective and efficient delivery of clinical development goalsSkillsBachelor or higher degree in a scientific or healthcare discipline with 10+ years' progressive experience in clinical trial industryProven project and program management experience in Early Phase clinical trials; First-In-Human experience favoredProven project management exposure/experience across the entire lifecycle of multi-region/country clinical trials in a fast-paced global environmentExperience in both people management and program management preferredExpert knowledge on the execution of clinical trials through a deep understanding of ICH/GCP Guidelines and other applicable regulatory requirementsStrong global program management skillsAbility to provide strategic leadership and managementExperience in building, developing and retaining a global teamAbility to oversee timely, quality, and efficient study planning and executionAbility to collaborate with cross-functional leaders to provide operational perspectivesStrong analytical thinking/data analysis skillsAbility to communicate with clarityOncology experience preferredExperience in both people management and program management preferredBenefitsNon-Commercial roles are eligible to participate in the annual bonus planCommercial roles are eligible to participate in an incentive compensation planAll Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awardsVoluntarily participate in the Employee Stock Purchase PlanThe Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and WellnessCompany OverviewBeOne Medicines is a global oncology company that is discovering and developing innovative treatments for cancer patients worldwide. It was founded in 2010, and is headquartered in Klein-basel, Basel-Stadt, CHE, with a workforce of 10001+ employees. Its website is https://beonemedicines.com.Company H1B SponsorshipBeOne Medicines has a track record of offering H1B sponsorships, with 3 in 2026, 20 in 2025. Please note that this does not guarantee sponsorship for this specific role.