Research Coordinator Jobs in Phoenix, AZ

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