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Senior Clinical Research Associate
Há 1 mês
We are seeking a Senior Clinical Research Associate to join our team at BeiGene. In this role, you will be responsible for conducting site visits, monitoring data quality and patient safety, and ensuring compliance with ICH-GCP guidelines.
About the RoleThe Senior CRA will assume the role of a primary CRA, conducting site visits, managing relationships with key site personnel, and ensuring effective communication. You will also be responsible for monitoring data quality and patient safety, as well as maintaining oversight of site performance.
Responsibilities- 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 related study training to assigned clinical study sites
- Maintain oversight of site performance by tracking metrics for enrollment, data entry into Case Report Forms (CRFs), protocol deviation trends, and overall site issues
- Serve as mentor/trainer for less experienced CRAs to assist with general and study-specific monitoring issues
To be successful in this role, you will need:
- Bachelor's degree in a relevant scientific discipline
- Minimum 2+ years of relevant Clinical Operations experience, and minimum 1+ years of monitoring experience
- Experience in global oncology trials preferred
- Excellent communication and interpersonal skills
- Excellent organizational skills and ability to prioritize and multi-task
- Fluent in English (writing and speaking)
This role requires up to 70% travel.
Salary InformationThe estimated salary for this position is $120,000 - $150,000 per year, depending on experience.