Arizonaliverhealth

Clinical Research Coordinator II/III

Chandler, AZ · Mid · Full-time

Sponsorship not specified$28k-$36kDetected 40 days ago

GCPComplianceRecruitingClinical TrialsClinical ResearchFDA RegulatoryPharmacovigilanceResearchCommunication

About the role

Arizona Clinical Trials is looking for qualified candidates for the Clinical Research Coordinator II / III position in Chandler
Title: Clinical Research Coordinator II or III
Responsible for coordinating and implementing assigned protocols in compliance with FDA CFR, GCP and company SOPs.

Under the direction of the Principal Investigator or sub-investigator, manage the conduct of clinical research activities.
Collects and records clinical research data, assists in patient assessments, scheduling, maintain study files, study supplies and study medication accountability.
Develop management systems and prepare for study initiation
We have an established and preferred network of contracted partners that we engage if and when we deem it necessary.

Plans, prepares and performs tasks required by protocol, which may include, but not limited to the following:
Shared company vehicles for required travel

Master's degree or study-specific training preferred
GCP certification required at hire.
Experience and training in the conduct of clinical research (specific experience and/or training in clinical research recruitment, including IRB submissions and trial enrollment management)
Experience with data management and tracking software
It is our policy that any and all contact with third party staffing or recruitment vendors come through our Talent Acquisition Team directly.
We request that staffing agencies refrain from repeatedly contacting our hiring managers or employees directly.
Overly persistent and pushy inquires may also be blocked across our network as spam.
Thank you for your understanding and cooperation.

Minimum (2) years of experience working previously as a Clinical Research Coordinator for late phase clinical trials.
A thorough understanding of regulatory requirements, principles of GCP and biomedical research ethics.
Know and understand all regulatory requirements associated with the conduct of the study assigned.

$27.50 to $36 per hour depending on experience and qualifications
Status: Full-time
Schedule: 7am - 4pm (Monday-Friday)
Essential job functions/duties:
Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.

Arizona Liver Health (ALH) is dedicated to driving high standards of care and advancing medical innovation through leading clinical trials, ensuring patient safety and regulatory compliance, and generating high-quality clinical data.
Our network of multiphase, multitherapeutic research, standard of care, and VEN Centers sites is staffed by skilled providers, research, clinic, pharmacy, and patient outreach professionals.
ALH operates state-of-the-art facilities and programs to meet the evolving needs of clinical research and overall patient treatment.

Participates in monitoring visits from sponsor provided appointees, ensures monitors are able to meet/speak with PI and ensures all concerns are addressed in a timely manner

This listing is sourced directly from Arizonaliverhealth's careers page and normalized into a canonical job model.