Director, Regional Clinical Study Management

BeOne Medicines; United States; On-site; USD 171,900 - 231,900; Full time

Benefits offered by this job

Comprehensive benefits package including Medical, Dental, and Vision

401(k)

Paid Time Off

Employee Stock Purchase Plan

Job summary

BeOne Medicines is seeking a seasoned leader in clinical operations, responsible for driving regional management and ensuring quality across studies. You will mentor clinical study managers and lead operational strategies to meet business goals.

The ideal candidate has 10+ years in clinical operations within biotech or pharmaceutical settings, demonstrating strong leadership, communication, and analytical skills. This role includes a competitive salary and comprehensive benefits.

Qualifications

• 10+ years of progressive experience in clinical operations within biotech, pharmaceutical, or CRO industry.
• Experience as direct line manager or cross-functional team lead.
• Strong judgement and ability to influence and lead.

Responsibilities

• Provide leadership and mentorship to clinical study managers.
• Drive resourcing and capability development for regional study management.
• Ensure adherence to quality expectations and processes.

Skills

Leadership

Communication Skills

Analytical Thinking

Project Planning

Interpersonal Skills

Education

Bachelor's degree in a scientific or healthcare discipline

Master’s degree in a scientific or healthcare discipline

Tools

MS Office

Project Planning Applications

Job description

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.

Line Management Responsibilities

• Provides leadership, management, and/or mentorship to associate directors, clinical study managers at various levels for assigned portfolio.
• Collaborates effectively with internal and external stakeholders within the region as well as with global stakeholders to ensure the needs of the business are met.
• Drives resourcing and capability development related to regional study management.
• Ensures alignment of regional resources and deliverables with overall portfolio goals.

Regional Leadership

• Provides leadership to the team of Associate Directors, Operations Managers, and Operations Associates in charge of regional study management, including mentoring, coaching and managing performance.
• Collaborates with peers in the regional Clinical Operations leadership team to ensure smooth delivery of all trials in the region on time, with quality and in line with the broader organizational goals.
• Liaises and collaborates as required with external, global and/or regional stakeholders such as e.g., FSP partners, clinical operations leaders in other regions, and monitoring heads in key countries in the region.
• Drives the overall Clinical Operations strategy for the region and has accountability for performance against key metrics.
• Drives the development of initiatives and ensures that novel ideas on how to deliver on clinical trials are generated and considered.

Quality

• Ensures team members are trained on and are adhering to required processes and SOPs.
• Drives a quality mindset in the regional study management organization and supports the proactive implementation of risk management principles in the regional study management organization.
• Sets clear quality expectations for the regional study management organization.
• Drives the knowledge management and continuous improvement process by ensuring information is captured, retained, and leveraged in future work.

Budget and Resources

• Contributes to the resourcing process for regional study management. Ensures efficient resourcing addressing both study needs as well as individual development needs through the principle of assigning the right person to the right study at the right point in time.

Supervisory Responsibilities

• Conducts performance appraisals for direct reports which includes providing feedback.
• Supports set up of development plans for direct reports.
• Drives the hiring of new talent into the regional study management organization.

Computer Skills

• MS Office, Project Planning Applications.

Other Qualifications

• Solid leadership and extensive experience either as direct line manager (required for those with line management responsibilities) or as cross functional team lead.
• Strong written and verbal communication skills.
• Exercises sound judgement and discretion in matters of significance.
• Ability to work independently and effectively handle multiple priorities in a fast‑paced environment.
• Excellent interpersonal skills, strong organizational skills and ability to influence and lead.

Travel

Travel might be required as per business need.

Education & Experience Required

Bachelor's degree in a scientific or healthcare discipline and 10+ years of progressive experience in clinical operations within biotech, pharmaceutical or CRO industry.

Preferably master’s degree in a scientific or healthcare discipline and 7+ years of progressive experience in clinical operations within biotech, pharmaceutical or CRO industry.

Global Competencies

• 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

Compensation

Salary Range: $171,900.00 - $231,900.00 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.

Equal Opportunity

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].