Regional Clinical Compliance Leader

BeiGene, Ltd.

Netherlands

Remote

EUR 89,000 - 111,000

Full time

14 days+
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Job summary

BeOne is seeking a Regional Clinical Compliance Country Manager to oversee country and site‑level trial compliance, ensuring adherence to GCP and internal standards. You will identify risks, guide CAPAs, and support inspections with Global Clinical Compliance partners.

The role requires a Bachelor’s degree in a scientific/medical field and 5+ years in clinical operations plus 4+ years in a GCP/compliance role, with oncology trial experience preferred. Travel ~20% is expected.

Qualifications

  • Understanding of clinical trial processes incl. ICH-GCP.
  • Analytical and problem‑solving skills.
  • High attention to detail and quality orientation.
  • Excellent communication and stakeholder management.
  • Excellent English written and verbal communication.
  • Excellent organizational skills and ability to prioritize/multitask.
  • Ability to work independently in a multi-cultural setting and handle multiple priorities.

Responsibilities

  • Serve as primary point of contact for country teams on GCP requirements and procedures.
  • Perform risk-based country/site oversight with data and process reviews.
  • Lead remote desk checks and coordinate with Clinical Ops and line managers.
  • Support CAPAs and issue management to ensure timely corrective actions.

Skills

Clinical processes awareness
Analytical/Problem-solving
Communication & stakeholder mgmt
English fluency
Organization & multitasking
Independent work in diverse team

Education

Bachelor’s degree in scientific/medical field

Tools

MS Office

Job description

BeOne is seeking a Regional Clinical Compliance Country Manager to oversee country and site‑level trial compliance, ensuring adherence to GCP and internal standards. You will identify risks, guide CAPAs, and support inspections with Global Clinical Compliance partners.

The role requires a Bachelor’s degree in a scientific/medical field and 5+ years in clinical operations plus 4+ years in a GCP/compliance role, with oncology trial experience preferred. Travel ~20% is expected.

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