Job Description
Overview:
- $60,000 - $70,000 salary based on experience
- Consistent M-F schedule, no overnights or weekends
- Benefits including Healthcare
About Our Client
Our client is a site network based in Arizona that specializes in conducting studies focused on liver diseases and metabolic conditions by partnering with world class pharmaceutical and biotech companies. They prioritize high-quality, patient-centered clinical trials and their mission is to improve health outcomes by contributing meaningful data to the development of innovative therapies.
Responsibilities
As a CRC you will be a specialized research professional under the direction of the clinical Principal Investigator and Site Manager. While the PI and Site Manager are responsible for the overall design, conduct, and management of the clinical trial, you support, facilitate, and coordinate the daily clinical trial activities and play a critical role in the conduct of the study including supporting patients throughout the clinical trial process!
- Conduct procedures such as vital signs, blood draws, EKGs, and scans
- Patient recruitment, enrollment, scheduling
- Informed consent
- Lab procedures and shipments
- Maintain GCP and follow protocols
- Data management in EDC systems
- Overall coordination of the study
- Study operations, work with site managers, PIs, and other staff
- Sponsor communications
- Regulatory management
Qualifications:
- 2+ years of experience working as a CRC on sponsor backed clinical trials
- Phlebotomy and lab processing experience (ability to perform without supervision)
- Ability to work on site M-F on site (there is no remote or hybrid days)