Oncology Clinical Research Manager (Associate)

BeiGene, Ltd.

United States

Remote

USD 106,000 - 141,000

Full time

7 days ago
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Benefits offered by this job

Medical
Dental
Vision
401(k)
Paid Time Off
Wellness

Job summary

BeOne Medicines Ltd. is seeking an Associate CRM to supervise the clinical monitoring team and ensure adherence to ICH-GCP, local regulations, and SOPs. The role combines team leadership with hands-on monitoring activities to deliver high-quality trial results.

You will allocate resources, guide CRA performance, and collaborate across functions to meet study milestones. A Bachelor’s degree in a science or healthcare field and 5+ years in pharma/CRO are required; oncology experience is strongly

Qualifications

  • 5+ years of industry experience in the pharmaceutical, CRO or related field.
  • Strong understanding of the drug development process and international standards (ICH-GCP).
  • Experience monitoring/trial execution and working knowledge of regulatory requirements.
  • Excellent interpersonal, organizational and written/verbal communication skills.
  • Oncology experience is highly recommended.

Responsibilities

  • Oversee clinical monitoring activities and CRA team performance to ensure ICH-GCP compliance and quality.
  • Lead recruitment, onboarding, task assignment and performance evaluation of team members.
  • Support site audits/inspections and ensure CAPA follow-up for identified issues.
  • Strengthen site relationships and risk management for trial delivery.
  • Collaborate with cross-functional teams to meet study milestones and provide guidance to team members.

Skills

Team leadership
Communication
Project management
Microsoft Office

Education

Bachelor’s degree in science or healthcare
Advanced degree preferred

Tools

Microsoft Word
Microsoft Excel
PowerPoint
Outlook

Job description

BeOne Medicines Ltd. is seeking an Associate CRM to supervise the clinical monitoring team and ensure adherence to ICH-GCP, local regulations, and SOPs. The role combines team leadership with hands-on monitoring activities to deliver high-quality trial results.

You will allocate resources, guide CRA performance, and collaborate across functions to meet study milestones. A Bachelor’s degree in a science or healthcare field and 5+ years in pharma/CRO are required; oncology experience is strongly

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