Executive Director, Head of Clinical Operations Excellence

Regulatory Jobs; United States; Remote; USD 272.000 - 352.000; Vollzeit

Zusammenfassung

BeOne Medicines Ltd. in the United States seeks a senior leader to advance Clinical Development and GCO strategies, ensuring GCP compliance, eTMF integrity, and streamlined operations across global trials.

You will build and mentor a capable team, drive KPI reporting, lead audits, CAPA management, and partner with QA, Corporate Compliance, and Development to deliver high-quality studies. This role requires deep regulatory knowledge, cross-functional influence and a track record of improving

Qualifikationen

• 15+ years in biotech/pharma/CRO in Clinical Operations, Clinical Compliance, Clinical Monitoring, Trial Management, or QA.
• Fluent in written and verbal English; Mandarin knowledge desirable.
• Strong leadership for cross-functional alignment and risk-based management.

Aufgaben

• Lead end-to-end clinical trial excellence oversight of SOPs and related processes.
• Develop, implement and revise SOPs; monitor compliance.
• Oversee eTMF platform and CAPA programs; ensure inspection readiness.

Kenntnisse

GCO leadership

Quality management

Regulatory compliance

Project management

SOP development

Training programs

Ausbildung

BS in scientific/healthcare

Tools

MS Word

Excel

Project

PowerPoint

Outlook

Jobbeschreibung

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 a member of the GCO Leadership team, contribute significantly to the development of Clinical Development & GCO strategies and provide expertise and leadership in the areas of process, eTMF managemnt, quality and compliance of all clinical operations conducted by the Global Clinical Operations Organization and its partners.
• Lead the development, implementation, and maintenance of a proactive GCP compliance management infrastructure/process, system within GCO, including clinical trial oversight processes, monitoring and quality control of key processes (eTMF), standard operating procedures and/or Work Instructions, training and change management .
• Build and lead a team with substantial capabilities to impact the continuous improvement of infrastructure and systems.
• Ensure adherence to regulatory requirements (ICH, FDA, EMA, PMDA, etc.) and GCP/PV guidelines through establishment and reporting of clinical performance indicators KPIs/KQIs, and through the use of innovative and agile methodology to improve processes.
• In collaboration with QA, Corporate Compliance, GCO & Development peers/associates, identify root causes for major and critical observations, devise relevant remedial and improvement actions for Corrective Action Plans, and follow-up on completion, implementation, and effectiveness of relevant tasks within GCO/Development.
• Develop GCO direct and indirect reports (e.g., Clinical Study Managers, CRAs…) to ensure greater value is added to the business across all areas and across regions.
• Inspire and lead efforts to deepen operations excellence within the Clinical Development and GCO organizations to drive faster, high quality clinical trials around the world.

Essential Functions of the Job:

• Member of the Global Clinical Operations Leadership team
• Participate in the development of Clinical Development & GCO strategies and provides expertise and leadership in the area of quality, compliance, and operations excellence in all aspects of clinical trials operations conducted by GCO and its partners (Clinical/Medical, Data Management, Clinical Supplies, PV, Statistics, QA, CROs, FSP, ...)
• Provide recommendations or ideas on how Global Clinical Operations’ programs can generate greater value for BeOne.

Procedures:

• Lead end-to-end clinical trial excellence oversight of Standard Operating Procedures.
• Develop, implement and revise SOPs. Monitor departmental compliance to established procedures and policies.
• Ensure operational processes, systems and standards are adopted and implemented consistently across trials.

Process Improvement

• Proactively Identify internal process improvements within GCO through monitoring of adequate Key Performance.
• Quality Indicators and assure that gaps are addressed appropriately in order to mitigate risk.
• Work in collaboration with Clinical Development functions as necessary.
• Explore and implement innovative ways, including standardization, to increase Clinical Operations excellence around the world; this in collaboration with BeOne Clinical Development and Applied Innovation functions.

Training:

• Develop training plans and programs across Global Clinical Operations and other clinical development functions as necessary.
• Actively monitor knowledge management by ensuring information is applied, retained, and leveraged for future work.
• Actively ensure Training compliance is best and meets Corporate and GCO goals.

Performance Metrics:

• Develop, Establish and Report clinical performance indicators KPIs/KQIs, which are related Quality and Complaince.
• Provide updates of performance and quality to the Clinical Development senior leadership and/or EC as necessary.

Compliance and eTMF:

• Develop, implement, and maintain the GCO Compliance Management Plan, including eTMF. Oversee the relationship with CQA to support and ensure compliance with GCP, SOP and Training requirements of the GCO organization. Support proactive monitoring and assessment of compliance risks. Prepare the organization for inspections.
• Identify emerging compliance concerns and review SOP deviations that impact GCO, conduct root cause analyses, and recommend solutions.
• Ensure assessment and resolution of all CAPAs are completed on time. Verify that appropriate CAPAs are implemented on all major and critical audit/inspections findings.
• Oversee processes and plans for development of relevant remedial and improvement actions for Preventative Action Plans from Audits/Inspections/Incidence and responsible for follow-up on completion and implementation of relevant tasks within GCO.

eTMF:

• Maintain and optimize the platform serving for eTMF .Leverage AI for further improving the efficiecy.
• Set up SOP and/or WI, lead the change maangement and oversight team’s actual performance on eTMF.
• Join in inspection preparation and conduction for securing the success on inspection.

Other functions but not limited to:

• Contribute to GCO and Clinical Trial Sourcing strategy development and take a lead role in vendor due diligence.
• Escalate issues to BeOne Senior Management team timely.
• Lead multi-functional, multi-national teams as it relates to quality conduct of clinical trials.

Supervisory Responsibilities:

• Direct and indirect line management.
• Manage internal staff and/or coordinate internal and external contractors/resources to maintain GCP compliance in the field organization as well as in the global GCO function.
• Mentor and coach the GCO teams as necessary.

Education Required:

• BS, with advanced degrees preferred, in a scientific or healthcare discipline.
• At least 15 years in the biotech/pharma/CRO industry in a relevant field of Clinical Operations, Clinical Compliance, Clinical Monitoring, Clinical Trial Management, and/or Clinical Quality Assurance.

Computer Skills:

• Efficient in Microsoft Word, Excel, Project, PowerPoint, and Outlook.

Other Qualifications:

• Fluent in written and verbal English. Desirable: knowledge of Mandarin.
• Excellent experience building GCP quality systems and process, including development of SOPs, effective CAPA programs.
• Strong leadership for driving the progress on cross-functional alignment.
• Risk based management skill and mindset.
• Skilled in Project Management, Root Cause Analysis, CAPA Management.
• Preferred experience with Six Sigma, LEAN, Agile methodologies.

Travel: Up to 25%

Global Competencies

When 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 Clarity

Salary Range: $271,800.00 - $351,800.00 annually

BeOne 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 [e-mail].