About UsBeOne 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.
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 DescriptionAccountable for regional study delivery with appropriate inspection readiness quality, within agreed timelines and budgetLeads the regional clinical operations team (including oversight of external partners working on the regional level) and acts as point of escalation for resolution of issues within the region for the assigned studyEnsures alignment of regional deliverables with overall study goalsLeads the regional clinical operations team effectively, ensures effective decision making and acts as point of escalation for resolution of issues within the region for the assigned studyLeads external vendors involved in study delivery on a regional levelCollaborates with key stakeholders in the region and provides regular updates on study progress in the region to senior management and Global Clinical Study Manager as requiredRepresents the regional study team at internal meetings and at the cross-functional Clinical Study Team (CST) meetingsLeads regional operations meetings with all regional study team membersLeads planning and management of the assigned clinical study(ies) from feasibility through closeout activities for region, in line with global study timelinesGenerates, manages, and maintains high quality study start up and recruitment timelines for region and tracks progress towards theseEnsures that the clinical study is operationally feasible in the region, drives trial feasibility, country allocation and site selection process for assigned region in collaboration with feasibility managers, country heads, medical affairs and any other stakeholdersProvides regional input on global study plans as requiredEnsures timely availability of local adaptations of global study documents such as informed consent forms,



in close collaboration with other key stake holders to ensure timely submission to regulatory authorities and ECs/IRBsAccountable for submissions of study in countries in assigned region in close collaboration with regional study start up team and regulatory affairsEnsures regional and country information in study systems and tools is entered and up to dateCollaborates closely with CRAs in the region to ensure proper study execution at the sites.
Reviews and signs-off monitoring reportsResponsible for working with regional and country teams to ensure that country and site level Trial Master File is created, maintained and QCd on a regular basis as per the study TMF QC planProvides input to Global Clinical Supplies regarding drug inventories in region and reviews local drug labels for region.
Provides input on local regulatory approval and reimbursement status of comparator drugs used in study for countries in regionManages the trial data collection process for the region, drives data entry and query resolutionAs required, supports planning and execution of the Clinical Study Report in collaboration with Global Clinical Study Manager and Medical WritingHandles escalated issues or problems with the sites in region in close collaboration with stakeholders such as country headsMonitors study activities in region to ensure compliance with the study protocol, SOPs, ICH/GCP and all other relevant regulationsEnsures inspection readiness for study in region at any point in time throughout the study life cycleInforms Global Clinical Study Manager of any issues arising on the study, evaluates impact and ensures solutions are implementedPrepares sites for quality assurance audits and inspections, drives responses to audit and inspection findings as appropriateCollaborates with CST members and colleagues to ensure cross-team, site learnings, and best practices are sharedLeads improvements and partners with CST members to enhance the efficiency and the quality of the work performed on assigned studiesContributes to development, optimization and review of work instructions and SOPs as requiredWorks with the sourcing team to select and manage regional study vendorsManages regional study budgetsWorks closely with Clinical Business Operation on investigator fees,



site payment issues and patient travel reimbursement activitiesIdentifies and manages regional team resource needs and establishes contingency plans for key resourcesMonitors regional resource utilization over study life cyle and liaises with functional managers as neededProvides performance feedback on team members as requiredMight mentor junior team membersQualification RequiredEducation Required: Bachelor's Degree in a scientific or healthcare discipline required, Higher Degree preferredComputer SkillsMS Office, Project Planning ApplicationsOther Qualifications4 or more years of progressive experience in clinical research within biotech, pharma or CRO industryProven experience in clinical research including relevant experience as team lead in clinicial functionsExperience as CRA is preferredWhat We Offer To Our Valued EmployeesMarket competitive compensation package including performance-based annual bonus schemeCompany shares (generous welcome grant!)In-house and external learning and development opportunitiesFantastic benefits program and keep improving!
Plus you get to work with a dynamic team of team-oriented, supportive, inclusive, and fun professionals whose mission is clear: Cancer has no borders and neither do we.Join us and Make momentum in your career!
BeOne Global CompetenciesFosters TeamworkProvides and Solicits Honest and Actionable FeedbackSelf-AwarenessActs InclusivelyDemonstrates InitiativeEntrepreneurial MindsetContinuous LearningEmbraces ChangeResults-OrientedAnalytical Thinking/Data AnalysisFinancial ExcellenceCommunicates with ClarityBeOne is committed to respect and protect personal information rights of job applicants and will process job applicants' personal information in accordance with applicable laws and regulations.
Due to BeOne's global operation, job applicants' data will be stored overseas with adequate protection.
Besides, job applicants' data will be stored for no longer than is necessary to facilitate potential application for other suitable positions in BeOne.
For further details, please refer to BeOne's Job Applicant Privacy Policy ( privacy-policy).
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📌 Regional Clinical Study Manager (New South Wales)
🏢 BeOne Medicines
📍 New South Wales