BeOne Medicines
BeOne Medicines
BeOne Medicines is a Switzerland-domiciled global oncology company focused on discovering and developing innovative cancer treatments designed to improve affordability and access. Its portfolio covers hematologic cancers and solid tumors, supported by an expanding pipeline of novel therapeutics advanced through in-house capabilities and external collaborations. With more than 11,000 colleagues across six continents, BeOne Medicines is working to broaden access to medicines for patients worldwide.

Associate Clinical Research Manager (Remote - United States)

Lead clinical trial monitoring, CRA performance, resource planning, and compliance activities for BeOne Medicines in a remote United States role. Support study delivery, team development, site relationships, audits, and risk resolution.

Description

  • Direct clinical monitoring activities and oversee CRA team performance
  • Maintain compliance with ICH-GCP, applicable regulations, and company SOPs
  • Guide the CRA team toward organizational objectives and strong performance
  • Plan CRA assignments and evaluate workloads to deliver study requirements
  • Ensure CRAs have the knowledge and skills to conduct high-quality monitoring
  • Track CRA performance and clinical quality indicators
  • Build effective site relationships that support trial performance and delivery
  • Evaluate monitoring quality and address compliance concerns
  • Coordinate with cross-functional teams to meet study and site milestones
  • Conduct assessment and accompanied visits when required
  • Detect operational issues and create practical resolution plans
  • Improve processes while managing risk escalation and issue resolution
  • Assist with site audits, inspections, and Site Compliance Visits
  • Drive corrective actions and follow-up for identified findings
  • Recruit, select, and onboard new team members
  • Delegate responsibilities according to individual capabilities and team priorities
  • Equip team members with the resources and support needed for success
  • Foster communication and collaboration across the team and other functions
  • Complete performance reviews and deliver constructive feedback
  • Coach team members and promote their professional growth
  • Resolve personnel matters promptly and equitably

Requirements

  • Proficiency with Microsoft Word, Excel, PowerPoint, and Outlook
  • Fluency in written and spoken English
  • At least five years of experience in pharmaceuticals, CROs, or a related industry
  • Comprehensive knowledge of the drug development process
  • Expertise in ICH-GCP standards and health authority requirements
  • Working knowledge of clinical monitoring and trial execution
  • Previous CRA experience is preferred
  • Strong interpersonal and relationship-building abilities
  • Highly organized approach to work
  • Clear and effective written and verbal communication
  • Oncology experience is highly recommended
  • Willingness to travel for business when required
  • Valid driver's license where applicable
  • Bachelor's degree or higher in a scientific or healthcare field
  • Advanced degree preferred

Benefits

  • Eligibility for an annual bonus plan in non-commercial roles
  • Eligibility for an incentive compensation plan in commercial roles
  • Discretionary equity awards
  • Optional participation in the Employee Stock Purchase Plan
  • Medical insurance
  • Dental insurance
  • Vision insurance
  • 401(k) plan
  • FSA/HSA
  • Life insurance
  • Paid time off
  • Wellness program

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