Senior Global Clinical Study Manager

BeiGene, Ltd.; United States; Remote; USD 136,000 - 181,000; Full time

Benefits offered by this job

Medical

Dental

Vision

401(k)

FSA/HSA

Life Insurance

Paid Time Off

Wellness

Job summary

BeOne Medicines Ltd. is seeking a Senior Global Clinical Study Manager to lead global study delivery from feasibility through closeout.

Remote (US) role with responsibility for timelines, budget, and inspection readiness, coordinating cross-functional teams and external partners to ensure high-quality trial delivery. You will oversee study planning, TMF, RBQM, site activation, and risk management, while aligning with clinical operations and program goals.

Qualifications

• 7+ years of progressive experience in clinical research within biotech, pharma or CRO.
• Bachelor’s degree in a scientific or healthcare discipline required.
• Oncology experience preferred and global study leadership capability.
• Ability to independently lead global clinical studies and ensure quality.
• Advanced knowledge of clinical operations methodologies and processes.

Responsibilities

• Lead the global cross-functional study team and external vendors.
• Plan and manage studies from feasibility through closeout with quality deliverables.
• Ensure study plans, TMF, data monitoring, and RBQM are in place and current.
• Monitor budgets, timelines, and resource needs; communicate to senior management.
• Maintain inspection readiness and drive process improvements across CST.

Skills

Global leadership

Clinical study management

Project management

Regulatory compliance

Vendor management

Education

Bachelor's degree in a scientific or healthcare discipline

Advanced degree preferred

Tools

MS Office

Clinical Trial Management Systems

Project Planning Applications

Job description

## Senior Global Clinical Study ManagerApply: Remote (US): Full time: Posted Today: R37260BeOne 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:**· Accountable for global study delivery within agreed timelines and budget with appropriate inspection readiness quality· Leads all aspects of assigned clinical study(ies)· Leads global cross-functional study team (including oversight of external partners) and acts as point of escalation for resolution of issues within assigned study(ies)· Ensures alignment of study goals with clinical operations and corporate goals and objectives· Contributes to development of global tools and standards, leads the development of work instructions and SOPs as required **Essential Functions of the job:****Cross-Functional Leadership**· Leads the global cross-functional study team effectively, ensures effective decision making, and acts as point of escalation for resolution of study related issues· Leads external vendors management involved in study delivery· Builds trust and relationship with regional subject matter experts and supports the delivery of their local study objectives· Collaborates with key stakeholders across the organization and provides regular updates on study progress to senior management as required · Represents the study team at internal meetings and leads the cross-functional Clinical Study Team (CST) meetings· Participates and presents at various topics of Clinical Study Management· Participates in Clinical Operations Process improvement initiative **Planning and Execution**· Leads planning and management of the assigned clinical study(ies) from feasibility through closeout activities· Generates, manages, maintains, and communicates high quality study timelines and tracks progress towards these· Ensures that the clinical studies are operationally feasible along with Global Clinical Program Lead, oversees trial feasibility, trial allocation and site selection process across all regions· Ensures timely availability of high-quality study documents to allow study submission to regulatory authorities and ECs/IRBs· Provides oversight to study start up and site activation plans· Ensures study plans (eg project management plan, monitoring plan, Trial Master File plan, data monitoring plan, ...) are created, updated and distributed timely and implemented appropriately· Ensures study systems and tools are set up timely, correctly and are functioning properly. Ensures study level information is updated on an ongoing basis in all systems· Implements RBQM end-to-end processes on time within the allocated study (e.g., periodic reviews, centralized monitoring analyses, action items)· Ensures relevant study specific training is developed and implemented and ensures training records are well documented and filed· Ensures Trial Master File for study is created, maintained and QC’d on a regular basis as per the study TMF QC plan· Collaborates closely with Global Clinical Supplies to forecast study drug and timely delivery of supplies to sites· Supports and as needed drives overall data cleaning timelines in close collaboration with Data Management and other stakeholders (including but not limited to regional clinical operations teams and medicator monitor)· Ensures planning and execution of the Clinical Study Report in collaboration with Medical Writing and relevant CST members **Quality and Risk Management**· Monitors study activities to ensure compliance with the study protocol, SOPs, all study plans, ICH/GCP and all other relevant regulations· Regularly reviews and manages quality-related GCO metrics to be within acceptable limits· Ensures inspection readiness at any point in time throughout the study life cycle· Works with cross-functional study team to identify, interpret, and evaluate issues on the study and ensures corrective and preventative actions are implemented· Ensures senior management and other key stakeholders are informed of risks and challenges and ensures risk mitigation plans are put in place and implemented· Prepares team for quality assurance audits and inspections · Collaborates with CST members and other colleagues to ensure cross-team, site learnings, and best practices are shared· Leads improvements and partners with study team members to enhance the efficiency and the quality of the work performed on assigned studies · Leads development, optimization and review of work instructions and SOPs as required **Budget and Resources**· Works with the sourcing team to select and manage study vendors, approving invoice payment throughout the study· Manages study budgets, including baseline budget evaluation, change control, study closure budget, presents study budget for senior management engagement · Adheres to clinical study budgeting processes and provides input to finance on budget accruals and forecasts· Identifies and manages study team resource needs and establishes contingency plans for key resources. · Monitors Clinical Study Team resource utilization over the study life cycle· Ensures clinical studies at a project level are executed within endorsed time, quality, and cost parameters**Supervisory Responsibilities:*** Mentors junior team members**Computer Skills:*** MS Office, Project Planning Applications, Clinical Trial Management Systems**Other Qualifications:**· Proven Project Management experience in Global Clinical Studies (Oncology experience preferred)· Advanced knowledge of clinical operations methodologies, in depth understanding of all aspects of clinical study processes· Able to independently lead global clinical studies · 7+ or more years of progressive experience in clinical research within biotech, pharma or CRO industry **Travel:**· Travel might be required as per business need.**Education Required:**· Bachelor’s Degree in a scientific or healthcare discipline required\\*, Higher Degree preferred*\\*exceptions might be made for candidates with relevant clinical operations experience*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 Teamwork* Provides and Solicits Honest and Actionable Feedback* Self-Awareness* Acts Inclusively* Demonstrates Initiative* Entrepreneurial Mindset* Continuous Learning* Embraces Change* Results-Oriented* Analytical Thinking/Data Analysis* Financial Excellence* Communicates with ClaritySalary Range: $136,400.00 - $181,400.00 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.