Regional Clinical Study Lead (Operations and Delivery)

BeOne Medicines Ltd.; Polska; On-site; PLN 325,000 - 406,000; Full time

Job summary

BeOne Medicines Ltd. is seeking a Regional Clinical Operations Lead to drive study delivery across the region in alignment with global timelines.

You will oversee the regional operations team and external vendors, ensuring feasibility, country allocation, site selection, and timely start-up activities. You will collaborate with country heads, medical affairs, and CST peers to maintain inspection readiness, manage budgets, and deliver high-quality data for regulatory submissions.

Qualifications

• Bachelor’s Degree in a scientific or healthcare discipline required; a Higher Degree is preferred.
• Minimum of 3–5 years of experience in clinical operations.
• Proven experience in clinical research, including team leadership in clinical functions.
• Experience as a Clinical Research Associate (CRA) is preferred.

Responsibilities

• Leads the regional clinical operations team effectively and acts as escalation point within the region.
• Leads external vendors involved in study delivery on a regional level.
• Collaborates with stakeholders in the region and provides updates to senior management and Global Clinical Study Manager.
• Represents the regional study team at CST meetings and internal meetings.
• Manages planning and execution of regional studies from feasibility through closeout.
• Ensures regional regulatory submissions and local documentation alignment with global plans.
• Monitors quality and ensures inspection readiness within the region.

Skills

Leadership

Clinical operations

Regulatory knowledge

Travel readiness

Education

Bachelor’s Degree in a scientific or healthcare discipline

Tools

MS Office

Project Planning Applications

Job description

BeOne Medicines Ltd. is seeking a Regional Clinical Operations Lead to drive study delivery across the region in alignment with global timelines.

You will oversee the regional operations team and external vendors, ensuring feasibility, country allocation, site selection, and timely start-up activities. You will collaborate with country heads, medical affairs, and CST peers to maintain inspection readiness, manage budgets, and deliver high-quality data for regulatory submissions.