The Clinical Research Coordinator II (CRC II) will be responsible for coordinating advanced clinical research projects proficiently with supervision, ensuring the integrity and quality of clinical research trials and compliance with all regulations and policies.
Requirements
- Assess eligibility of potential subjects through screening interviews, medical records, and discussions with physicians and nurses
- Maintain required records of study activity, including case report forms and regulatory forms
- Perform standard accounting functions, monitor and review accounting reports, and prepare and review budget and invoices
- Direct the requisition, collection, processing, labeling, storage, or shipment of specimens
- Monitor study activities to ensure compliance with protocols and regulations
- Schedules subjects for appointments and procedures as required by study protocols
- Assist with preparing IRB submissions, protocol revisions, and renewals
Benefits
- Competitive salary
- Benefits package
- Opportunities for career growth