The Senior Clinical Research Associate is responsible for managing assigned clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP guidelines
Job Summary
The Senior Clinical Research Associate is responsible for managing assigned clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP guidelines.
This role involves proactively seeking opportunities to lead improvements within the Site Management group and providing direct mentorship to junior CRA team members.
BeOne offers a comprehensive benefits package including medical, dental, vision, 401(k), life insurance, paid time off, and discretionary equity awards.
Matching Summary
The Senior Clinical Research Associate is responsible for managing assigned clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP guidelines.
Salary
Base: $105,800.00 - $140,800.00 annually; Bonus/Equity: Eligible for annual bonus plan and discretionary equity awards; Benefits: Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, Wellness
Skills & Requirements
Must-have
ICH-GCP guidelines knowledge
3-4 years CRA monitoring experience
Site visit coordination and documentation
SAE reconciliation and resolution
Protocol and regulatory compliance
Nice-to-have
Mentoring less experienced CRAs
Global oncology trial experience
Dashboard review and risk assessment
Audit/inspection preparation support
Collaborative spirit and initiative
Key Requirements
BS/BA in relevant scientific discipline
Minimum 4-6 years Clinical Operations experience
Minimum 3-4 years CRA monitoring experience
Thorough knowledge of ICH and regulatory guidelines