Lead Clinical Research Associate – Oncology Trials

BeOne Medicines Ltd.

United States

On-site

USD 92,000 - 122,000

Full time

3 days ago
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Benefits offered by this job

Annual bonus plan
Incentive compensation plan
Equity awards
Employee Stock Purchase Plan
Comprehensive benefits package

Job summary

BeOne Medicines is seeking an experienced Clinical Research Associate (CRA) to lead monitoring activities as a primary CRA, conduct site visits (PSSV, SIV, IMV, COV) and maintain communications with investigative sites.

You will monitor data quality and patient safety per ICH-GCP, train sites, track enrollment and CRF data, and support audits. Travel up to 70% and a competitive salary with benefits, including bonus eligibility.

Qualifications

  • Fluent English (writing and speaking).
  • Excellent communication and interpersonal skills.
  • Excellent organizational skills and ability to prioritize and multi-task.
  • Experience with CTMS and data management systems is preferred.

Responsibilities

  • Perform and coordinate clinical monitoring in accordance with GCPs and SOPs to assess safety and efficacy.
  • Conduct site visits to verify protocol and regulatory compliance and prepare documentation.
  • Develop relationships with investigative sites and study vendors.
  • Provide protocol and study training to CRAs and sites.

Skills

Fluent English
Excellent communication
Organizational skills
Team collaboration

Education

BS/BA in relevant scientific discipline

Tools

Microsoft Word
Excel
PowerPoint
Outlook
CTMS

Job description

BeOne Medicines is seeking an experienced Clinical Research Associate (CRA) to lead monitoring activities as a primary CRA, conduct site visits (PSSV, SIV, IMV, COV) and maintain communications with investigative sites.

You will monitor data quality and patient safety per ICH-GCP, train sites, track enrollment and CRF data, and support audits. Travel up to 70% and a competitive salary with benefits, including bonus eligibility.

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