Clinical Research Coordinator II or III; CRC Peoria

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.

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.

Arizona Liver Health/Arizona Clinical Trials is looking for qualified candidates for the Clinical Research Coordinator II or III position in Peoria

Title: Clinical Research Coordinator II or III (CRC 2 or
3)

Compensation: $27.50 to $36 per hour, depending on experience

Status: Full-time, Non-exempt, Hourly

Location: Peoria, AZ (N. 83rd Ave.)

Schedule: Monday-Friday, 7am-4pm (set schedule)

Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.

• Under the direction of the Principal Investigator or sub-investigator, manage the conduct of clinical research activities.
• Responsible for coordinating and implementing assigned protocols in compliance with FDA CFR, GCP and company SOPs.
• 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
• Review with the Principal Investigator the inclusion/exclusion criteria, overall structure and requirements of each protocol
• Review the protocol summary sheet and the Informed Consent Form for accuracy and clarity about these protocols to staff and patients.
• Responsible for the recruitment and screening of potential participants, which includes chart review of patients and schedules, contacting leads from outside recruitment efforts, and following up on referrals from all sources.
• Responsible for meeting recruitment goals for each study.
• May assume primary responsibility in the implementation and management of new clinical trials in a knowledgeable and collaborative manner.
• Performs all functions according to established policies (SOPS), procedures, regulatory and accreditation requirements, as well as applicable professional standards.
• Provides educational information to subjects. Serves as a resource and support person for subjects and families by being a consistent person they can contact within the clinical research program.
• Provides all employees and research subjects with an excellent service experience by consistently demonstrating professional decorum.
• Serves as a liaison to all physicians, employees, and third-party vendors.
• Record data and study documentation
• Keep the clinical trial management system updated with newly recruited subjects, tracking completed visits and stipends for the participants and investigators and ensuring status of each patient is accurate.
• Assign patient stipend pay card at screening
• Document reason for screen-fail in real time
• Plans, prepares and performs tasks required by protocol, which may include, but not limited to the following:
• Record data as directed using the appropriate media or platform
• Follow procedures for access and security for electronic data entry
• Review keyed data for accuracy as needed
• Send data to the data collection center on a timely basis
• Maintain source documentation for all data entered, including clinic chart visit notes, lab data and procedure reports
• Develop and/or edit source as needed independently or with Quality Assurance / Quality Control team to ensure compliance with protocol and EDC.
• Correct and edit data as directed and as appropriate.
• Informed Consent
• Obtaining patient medical history and medication lists
• Phlebotomy and basic laboratory tests
• Processing & shipping labs for…