Associate Clinical Research Manager | Team Lead

BeOne Medicines Ltd.

San Mateo (CA)

On-site

USD 130,000 - 180,000

Full time

6 days ago
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Job summary

BeOne Medicines Ltd. seeks an Associate CRM to oversee clinical monitoring activities and lead the CRA team in line with ICH-GCP and company SOPs. The role guides performance, provides development opportunities, and fosters a positive team culture in a dynamic environment.

As a manager, you will allocate resources, drive quality across trials, and collaborate with cross-functional teams to ensure milestones are met. Oncology experience is highly recommended and travel may be required.

Qualifications

  • Bachelor’s degree or higher in a scientific or healthcare discipline.
  • Minimum 5 years of industry experience in the pharmaceutical or CRO field.
  • Thorough understanding of ICH-GCP and health authority requirements.
  • Understanding of monitoring and trial execution; CRA experience preferred.
  • Experience in Oncology is highly recommended.

Responsibilities

  • Allocate CRA resources and assess workload to meet study deliverables with quality monitoring.
  • Ensure CRA performance and quality indicators align with ICH-GCP, SOPs and local regulations.
  • Recruit, onboard, develop and mentor team members; manage performance and growth.
  • Promote cross-functional collaboration and act as a point of contact for issue escalation.
  • Support site audits/inspections and corrective action follow-up.
  • Travel as required for business needs.

Skills

Team leadership
Communication
Project management
Regulatory knowledge
Quality & compliance

Education

Bachelor’s degree in science/healthcare

Tools

Microsoft Word
Excel
PowerPoint
Outlook

Job description

BeOne Medicines Ltd. seeks an Associate CRM to oversee clinical monitoring activities and lead the CRA team in line with ICH-GCP and company SOPs. The role guides performance, provides development opportunities, and fosters a positive team culture in a dynamic environment.

As a manager, you will allocate resources, drive quality across trials, and collaborate with cross-functional teams to ensure milestones are met. Oncology experience is highly recommended and travel may be required.

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