Phoenix, Arizona, United States
Schedule & Compensation
• Full-time, on-site at the Phoenix-area research clinic
• Compensation based on experience
• 4 weeks PTO annually
• Up to 2 weeks sick leave for self, plus up to 2 weeks for family care
• Eligible for health, dental, vision, short term disability, long term disability insurance benefits
• Strong overall work-life balance
Responsibilities
• Support day-to-day conduct of Phase Ib/IIa proof-of-concept clinical trials, working alongside nurses, Sub-Investigators, and project managers
• Partner closely with clinic nurses, who also carry some CRC-type responsibilities, and provide backup support for nursing tasks as needed
• Screen, consent, and schedule study participants in line with protocol requirements
• Maintain accurate source documentation and case report forms
• Assist with startup and regulatory tasks as needed (lighter regulatory load, as project managers lead this area)
• Manage study supplies, lab kits, and specimen handling/shipping
• Track patient recruitment and retention against enrollment targets
• Stay flexible and adaptable as the clinic grows and systems continue to develop
Why This Role
✓ Join a specialized clinic focused exclusively on early-phase, proof-of-concept trials
✓ Be part of a growing US presence for an established international research network
✓ Work as part of a close-knit team alongside nurses, Sub-Investigators, and project managers
✓ Help shape processes and systems as the clinic grows
Qualifications
• Bachelor's degree in a life sciences, nursing, or related field a plus
• 1+ years of clinical research coordination experience preferred
• CCRC/CCRP, phlebotomy, or Medical Assistant certification a plus
• Working knowledge of GCP/ICH guidelines and FDA regulations
• Comfortable working directly with patients in a clinical setting
• Flexible, patient, and comfortable with evolving processes in a growing clinic