Senior Director, Regional Clinical Study Management

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 part of the regional leadership team, provides inspirational leadership, proactive management, and feedback-oriented mentorship to clinical study managers at various levels for assigned portfolio and may lead a designated therapeutic area or assetAccountable for regional study or portfolio delivery with appropriate inspection readiness quality, within agreed timelines and budgetMay act as regional lead (if needed) for one or multiple studies across an indication or across a program as required.Leads regional clinical operations teams (including external partners working on a regional level) and acts as point of escalation for resolution of issues within the region for the assigned portfolio of studies.Ensures alignment of regional resources and deliverables with overall portfolio goals.Creates an environment that fosters innovation of regional tools and leads the development of work instructions and SOPs as required.Drives deliverables regionally for trial or portfolio.Essential Functions of the job:Regional LeadershipInfluences improved standards of quality and efficiency for the region, promoting subject matter, disease area, or asset level expertise.Strategically leads the regional clinical operations team effectively across the department, ensures effective decision making and acts as point of escalation for resolution of issues within the region for the assigned study.Collaborates with key stakeholders in the region and provides regular updates on portfolio progress in the region to senior management and Global Clinical Study Manager as required.Champions high-impact, cross-departmental teams within and across the region to ensure different perspectives, ideas and expertise are reflected when executing clinical trialsDevelops, refines, and articulates regional goals, inspiring performance across teams, and develops cross-functional strategies that lead to portfolio success.Displays therapeutic area knowledge and expertise of assigned portfolio and encourages individuals across the region to aspire to develop this expertise.Timelines, Planning and ExecutionOversees the planning and management of the assigned clinical studies from feasibility through closeout activities for region, in line with global study timelines.Influences regional leaders to generate, manage, and maintain high quality study start up and recruitment timelines for region and tracks their progress to plan.Shapes and influences strategies to ensure that the clinical studies are operationally feasible in the region, optimizes trial feasibility, country allocation and site selection process for assigned region in collaboration with feasibility managers, country heads, medical affairs and any other stakeholders.Provides regional input on global study plans that refine their templates.Drives a feedback-oriented culture, in which regional study managers are held accountable for effective coaching and mentoring CRAs to ensure proper study execution at the sites.Provides 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 region.Understanding the big picture, sets expectations and anticipates and drives the trial data collection process for the region, and influences regional study managers to improve metrics on data entry and query resolution.As required, oversees the planning and execution of the Clinical Study Report in collaboration with Global Clinical Study Manager and Medical Writing.QualitySets clear quality expectations and priorities for the regional study management and strategies to achieve these expectations.Anticipates potential concerns and resolves escalated issues or problems with the sites in region in close collaboration with stakeholders such as country heads.Monitors study activities in region to ensure compliance with study protocol, SOPs, ICH/GCP and all other relevant regulations.Ensures inspection readiness for studies in region at any point in time throughout the study life cycle.Engages effectively across the regional leadership to ensure cross-team, site learnings, and best practices are shared, promoting awareness and cross-functional collaborations.Improves workload management by supporting clinical study managers in setting priorities and by postponing less relevant workLeads the development, optimization and review of work instructions and SOPs as required.Budget and ResourcesDemonstrates understanding of the department’s business levers that impact financial goals, and employs that knowledge to make critical business decisions for the department that support the region’s financial goalsWorks with the sourcing team to strategize regional study vendor needs.Works closely with Clinical Business Operation on optimizing efficiency related to investigator fees, site payment issues and patient travel reimbursement activities.Strategically forecasts regional team resource needs and establishes contingency plans for key resources.Optimizes regional resource utilization over study lifecycle and liaises with functional managers as needed.Supervisory Responsibilities:As part of the regional leadership team:Interviews, line manages, and evaluates performance of regional clinical study managers (rCSMs)Will support regional strategy and provide input on resourcing assignmentsProvides key input on annual operating plan, headcount, and budgetCommunicates with FSP partnersInspires individuals across the business unit to perform at their best; encourages others to recognize their contributions toward the success of the business unit and stay motivatedEnsures the competencies and skills required for the regional Clinical team are consistent with the company defined requirements.Develops and implements effective coaching and mentoring processes that can be customized to support both junior team and senior team members and supporting their professional development plans.Conduct performance appraisals for direct reports which includes providing feedback.Computer Skills:MS Office, Project Planning ApplicationsOther Qualifications:Proven experience in clinical research including relevant experience as team lead in clinical functions and experience across multiple studies preferred.Travel:Travel might be required as per business need.Education & Experience Required: Bachelor's degree in a scientific or healthcare discipline and 12+ years of progressive experience in clinical operations within biotech, pharmaceutical or CRO industry. Preferably master’s degree in a scientific or healthcare discipline and 8+ years of progressive experience in clinical operations within biotech, pharmaceutical or CRO industry.Global CompetenciesWhen we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.Fosters TeamworkProvides and Solicits Honest and Actionable FeedbackSelf-AwarenessActs InclusivelyDemonstrates InitiativeEntrepreneurial MindsetContinuous LearningEmbraces ChangeResults-OrientedAnalytical Thinking/Data AnalysisFinancial ExcellenceCommunicates with ClaritySalary Range: $206,200.00 - $276,200.00 annuallyBeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans’ Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact View email address on click.appcast.io. #J-18808-Ljbffr BeiGene, Ltd.