Senior CRA II | Remote Oncology Trials

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

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k)

FSA/HSA

Life Insurance

Paid Time Off

Wellness program

Job summary

BeOne Medicines Ltd. is seeking a Clinical Research Associate II to join our remote US team. The role involves performing site visits, monitoring data quality, and coordinating clinical monitoring activities in line with ICH-GCP guidelines.

You will build relationships with investigative sites, train site staff, and mentor junior CRAs while ensuring study milestones and quality standards are met. Strong communication and organization are essential.

Qualifications

• BS/BA in a relevant scientific discipline and minimum of 2+ years of Clinical Operations experience, and minimum of 1+ years of monitoring experience.
• Excellent communication and interpersonal skills.
• Fluent in English (writing and speaking).

Responsibilities

• Perform and coordinate assigned aspects of the clinical monitoring process in accordance with GCPs and SOPs to assess safety and efficacy of investigational products.
• Conduct site visits to determine protocol and regulatory compliance, and prepare required documentation.
• Develop collaborative relationships with investigative sites and study vendors.
• Provide protocol and study training to assigned sites.
• Attend disease indication and project-specific training as required.
• Maintain oversight of site performance by tracking enrollment, data entry into CRFs, protocol deviation trends, and site issues.

Skills

Communication

Interpersonal skills

Organization

Fluent English

Education

BS/BA in a relevant scientific discipline

Tools

Microsoft Word

Excel

PowerPoint

Outlook

CTMS

Data management systems

Job description

BeOne Medicines Ltd. is seeking a Clinical Research Associate II to join our remote US team. The role involves performing site visits, monitoring data quality, and coordinating clinical monitoring activities in line with ICH-GCP guidelines.

You will build relationships with investigative sites, train site staff, and mentor junior CRAs while ensuring study milestones and quality standards are met. Strong communication and organization are essential.