On-Site Clinical Research Coordinator – Phoenix Trials

ARENSIA Exploratory Medicine USA; Phoenix (AZ); On-site; USD 55,000 - 75,000; Full time

Job summary

ARENSIA Exploratory Medicine USA is seeking a Clinical Research Coordinator for our Phoenix, AZ clinic. This full-time, on-site role manages day-to-day trial activities, including participant screening, enrollment, scheduling, and visit management, while ensuring adherence to protocol and regulatory standards.

You will collaborate with investigators, nurses, sponsors, and CROs, handling source documents, data entry, safety monitoring, and audits to drive smooth trial operations and a positive

Qualifications

• Hands-on involvement in clinical trials and study operations.
• Explain study information clearly to participants.
• Implement protocol requirements in daily practice.
• Work within GCP/ICH regulatory standards.
• Education in health sciences; certification in clinical research is a plus.
• Excellent organization and attention to detail.
• Strong written and verbal communication; interact with participants, investigators, sponsor reps.
• On-site in Phoenix, AZ; fast-paced early-phase environment.

Responsibilities

• Coordinate participant screening, enrollment, scheduling, and visit management.
• Ensure adherence to study protocols and regulatory files.
• Manage informed consent processes and source documentation.
• Support study assessments and sponsor/CRO communications.
• Assist with monitoring visits, audits, and site improvements.

Skills

Clinical research

Informed consent

Study protocols

GCP compliance

Communication skills

Organizational skills

Multitasking

Early-phase research

Education

Health sciences / nursing / biology or related field; clinical research certification (e.g., CCRC)

Job description

ARENSIA Exploratory Medicine USA is seeking a Clinical Research Coordinator for our Phoenix, AZ clinic. This full-time, on-site role manages day-to-day trial activities, including participant screening, enrollment, scheduling, and visit management, while ensuring adherence to protocol and regulatory standards.

You will collaborate with investigators, nurses, sponsors, and CROs, handling source documents, data entry, safety monitoring, and audits to drive smooth trial operations and a positive