Senior Clinical Research Associate

BeOne Medicines

Senior Clinical Research Associate responsible for oversight of clinical study sites in BeOne's oncology trials. Collaborating to ensure data quality and patient safety under established protocols.

Posted 5/19/2026full-timeRemote • 🇺🇸 United StatesSenior💰 $105,800 - $140,800 per yearWebsite

About the role

Key responsibilities & impact

Perform and coordinate assigned aspects of the clinical monitoring process in accordance with GCPs and SOPs to assess the safety and efficacy of investigational products and/or medical devices
Conduct site visits to determine protocol and regulatory compliance, and prepare required documentation
Develop collaborative relationships with investigative sites, and study vendors
Track enrollment status reports to ensure study sites stay on track to meet enrollment goals
Serve as mentor/trainer for less experienced CRAs to assist with general and study-specific monitoring issues
Provide direct support to the Clinical Study Manager by assisting with monitoring visit report review and other managerial tasks as needed
Perform Serious Adverse Event (SAE) reconciliation and work with study sites and CRAs to resolve discrepancies
Collaborates with CST and clinical study sites to ensure timely delivery of study milestones.

Requirements

What you’ll need

Minimum of 4-6 years of relevant Clinical Operations experience
Minimum of 3-4 years of (CRA) monitoring experience in the pharmaceutical or CRO Industry
Excellent communication and interpersonal skills
Excellent organizational skills and ability to prioritize and multi-task.

Benefits

Comp & perks

Medical
Dental
Vision
401(k)
FSA/HSA
Life Insurance
Paid Time Off
Wellness

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

clinical monitoringGCPSOPprotocol complianceregulatory complianceSAE reconciliationmonitoring visit report review

Soft Skills

communicationinterpersonalorganizationalprioritizationmulti-taskingmentoringcollaboration