Senior Clinical Research Associate - Oncology Trials

BeiGene Ltd.; United States; Remote; USD 92,000 - 122,000; Full time

Benefits offered by this job

Annual bonus plan

Equity awards

Benefits package

Paid time off

Job summary

BeOne Medicines Ltd. is seeking a dedicated Clinical Research Associate (CRA) to serve as a primary CRA, conducting site visits and acting as a site manager.

You will monitor data quality and patient safety, ensuring adherence to ICH-GCP and SOPs across global oncology trials. Travel up to 70% and strong communication are essential as you develop relationships with investigative sites and provide training to site staff.

Qualifications

• BS/BA in a relevant scientific discipline with 2+ years of Clinical Operations experience and 1+ year of monitoring experience.
• Experience in global oncology trials preferred.
• Fluent in English (writing and speaking).

Responsibilities

• Perform and coordinate clinical monitoring per GCPs and SOPs to assess safety/efficacy of investigational products or devices.
• Conduct site visits to ensure protocol and regulatory compliance and prepare required documentation.
• Develop collaborative relationships with investigative sites and study vendors.
• Provide protocol and study training to assigned clinical study sites.
• Maintain oversight of site performance by tracking enrollment and data entry in CRFs.

Skills

Communication skills

Interpersonal skills

Fluent English

Team collaboration

Education

BS/BA in a scientific discipline

Tools

CTMS

Data management systems

Job description

BeOne Medicines Ltd. is seeking a dedicated Clinical Research Associate (CRA) to serve as a primary CRA, conducting site visits and acting as a site manager.

You will monitor data quality and patient safety, ensuring adherence to ICH-GCP and SOPs across global oncology trials. Travel up to 70% and strong communication are essential as you develop relationships with investigative sites and provide training to site staff.