TEMPORARY - Clinical Research Coordinator III (CRC3) Peoria

 

About Us:

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.

 

Job Summary:

Arizona Liver Health/Arizona Clinical Trials is looking for qualified candidates for the TEMPORARY - Clinical Research Coordinator III position in Peoria.

Title: TEMPORARY - Clinical Research Coordinator III (CRC3)

Compensation: $40-$45 per hour, depending on experience

Status: Full-time, 3-Month Contract (eligible for overtime)

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

Start date: July 7th, July 14th or ASAP 

(1 opening)

Essential job functions/duties:

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.
• Screen and enroll study subjects
  • Review the study design and inclusion/exclusion criteria with the subject’s primary physician
  • Review and verify all relevant source documentation in the subject's medical record to confirm study eligibility
  • Review the protocol, Informed Consent Form, and follow-up procedures with potential study subjects
  • Ensure the current approved Informed Consent is signed before subjects are screened and enrolled
  • Ensure that the randomization procedure is followed as per protocol guidelines
  • Document protocol exemptions and deviations.
  • Ensures that primary referring physicians receive timely progress notes.
  • Ensures uniform implementation of protocols by completing required training documentation in a consistent, accurate and timely manner.
  • Ensure the delegation logs are correct and only delegated site staff are performing duties as listed on the delegation log for any given study.
  • Assists in regulatory functions, including but not limited to preparing appropriate Institutional Review Board (IRB) forms, processing updated informed consents, protocols, correspondence, and regulatory filing in an accurate and timely manner.
• Manage study-related activities, subject compliance and documentation
  • Ensure adherence to protocol requirements
  • Schedule subjects for follow-up visits
  • Assist investigators in assessment of subject response to therapy
  • Review laboratory data, inform investigator of abnormal values and document
  • Report to primary care provider as appropriate
  • Assess and document subject compliance with medications and visits
  • Commu