TEMPORARY - Clinical Research Coordinator - Peoria

TEMPORARY

• Clinical Research Coordinator
• Peoria Arizona Liver Health
• 3.

2 Peoria, AZ Job Details Temporary | Full-time | Contract $35 an hour 2 hours ago Benefits Mileage reimbursement Qualifications Medication dispensing Computer operation Vital signs Calibration Adverse event reporting Labeling Healthcare Administration Filing Research Mid-level ECG equipment 3 years Patient safety High school diploma or GED Data quality management Bachelor's degree in health sciences Schedule management Key Performance Indicators Quality assurance audits ICH guidelines Clinical staff training Collecting samples for laboratory testing Bachelor's degree Medication supplies Staff training Health Science Data entry Research compliance clinical trial records management Quality control operations Bachelor's degree in healthcare administration Patient recruitment Regulatory submissions Patient interaction Typing Research regulatory compliance IATA Certification Quality audits IRB compliance Regulatory audits Pharmaceutical inventory management Communication skills FDA regulations

Full Job Description 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 position in

Peoria Title:

TEMPORARY

•

Clinical Research Coordinator Compensation:

$35 / hour (set rate)

Status:

Full-time, 40 hours, 4-Month Contract (eligible for overtime)

Work Schedule:

Monday-Friday, 7am-4pm (set schedule) Start date: June 15th or June 29th Open to permanent role consideration at the end of the contract period, depending on business need (4 openings) Essential job functions/duties Reasonable accommodation may be made to enable individuals with disabilities to perform these essential functions.

Participant Recruitment & Enrollment:

Identify, screen, and recruit eligible participants according to study protocol and inclusion/exclusion criteria. Conduct informed consent process and ensure documentation is complete and properly stored. Maintain participant retention efforts; schedule and follow up with participants for visits and assessments.

Research Procedures & Clinical Duties:

Phlebotomy:

collect, label, process, and ship blood and other biospecimens as required.

Pharmacy Tech:

assist with investigational drug handling, storage, dispensing, accountability logs, and inventory management of study medications or investigational products as permitted. Take vital signs, height/weight measurements, ECGs (if applicable), and other protocol‐specified assessments Follow study procedures to ensure participant safety, monitor adverse events (AEs) and serious adverse events (SAEs), report as required.

Data Management & Entry:

Enter data accurately into source documents and electronic databases / Electronic Data Capture (EDC) systems. Maintain, update, and monitor case report forms (CRFs), sponsor forms, regulatory files, source documentation.

Query resolution:

respond to data queries from monitors or sponsors in a timely manner. Ensure data integrity, consistency, and completeness.

Regulatory Compliance & Documentation:

Prepare, maintain, and submit regulatory documents in collaboration with the internal Regulatory team: Institutional Review Board (IRB) submissions, amendments, renewals. Ensure study compliance with Good Clinical Practice (GCP), FDA, ICH, or other applicable regulatory guidelines. Manage study files, regulatory binders, SOPs (standard operating procedures), study protocols. Participate in monitoring visits, audits, and ensure corrective action of findings.

Study Operations & Coordination:

Conduct all patient visits for assigned studies and follow all standard operating procedures (SOPs) accurately as outlined in study protocol. Meet key performance indicators (KPIs) regarding visit goals Schedule study visits and ensure all protocol procedures are done on schedule. Report all Significant Adverse Events (SAEs) in a timely manner Collaborate with labs, pharmacies, imaging, vendors, sponsors, and internal clinical staff to ensure smooth execution of trial procedures. Maintain inventory of supplies and study materials; ensure equipment is calibrated and functioning. Assist in managing investigator meetings, site initiation, close‐out visits. Additional duties to be assigned to role as applicable: Conduct Clinical Research study visits when assigned Communicate with sponsors effectively and professionally and in a timely manner to resolve issues or provide updates as needed Provide guidance as needed for CRC level I staff Audit research trials Perform vital signs, arthrometric measurements, transient elastography, and EKG's Quality control research visits and informed consent before screening visit is over Confirm correct IP prior to dispensation File the signed copy in the subject binder(s) Knowledge/Skills/Abilities Required Good knowledge of commonly used concepts, practices, and procedures in Research field Strong attention to detail Excellent communication skills Strong data management skills Excellent bedside management/patient communication skills Ability to train junior staff members (CRC I's) as needed Supervisory responsibilities None Work environment Clinic setting Physical demands Able to lift at least 15 lbs. Able to sit for long periods (at least 50%) Able to type and do computer work for long periods Travel Requirements Some interoffice travel may be required with use of company vehicle or mileage reimbursement Education, credentials, and/or trainings required High School Diploma or GED required from an accredited institution Good Clinical Practice (GCP) certification (can be completed upon hire) IATA certification (can be completed upon hire) Bachelor's degree in health sciences, healthcare administration, healthcare compliance, or related field preferred 3 years of experience in the field or in a related area Work authorization Must have valid documentation and authorization to work in the U.S., visa sponsorship or transfer is not available Affirmative Action/EEO statement It is the policy of the Institute for Liver Health DBA Arizona Liver Health and Arizona Clinical Trials to provide equal employment opportunities without regard to race, color, religion, sex, national origin, age, disability, marital status, veteran status, sexual orientation, genetic information, or any other protected characteristic under applicable law. This policy relates to all phases of employment, including, but not limited to, recruiting, employment, placement, promotion, transfer, demotion, reduction of workforce and termination, rates of pay or other forms of compensation, selection for training, the use of all facilities, and participation in all company-sponsored employee activities. Provisions in applicable laws providing for bona fide occupational qualifications, business necessity or age limitations will be adhered to by the company where appropriate. Other duties Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Other responsibilities may be communicated directly by the reporting manager/supervisor. Duties, responsibilities, and activities may change at any time with or without notice. EEO statement It is the policy of the Institute for Liver Health DBA Arizona Liver Health and Arizona Clinical Trials to provide equal employment opportunities without regard to race, color, religion, sex, national origin, age, disability, marital status, veteran status, sexual orientation, genetic information or any other protected characteristic under applicable law. This policy relates to all phases of employment, including, but not limited to, recruiting, employment, placement, promotion, transfer, demotion, reduction of workforce and termination, rates of pay or other forms of compensation, selection for training, the use of all facilities, and participation in all company-sponsored employee activities. Provisio=ns in applicable laws providing for bona fide occupational qualifications, business necessity or age limitations will be adhered to by the company where appropriate. Notice to

Staffing Agencies:

It is our policy that any and all contact with third party staffing or recruitment vendors come through our Talent Acquisition Team directly. We have an established and preferred network of contracted partners that we engage if and when we deem it necessary. We request that staffing agencies refrain from repeatedly contacting our hiring managers or employees directly. Unsolicited resumes, onsite solicitations, and inquiries will not be considered or responded to. Overly persistent and pushy inquires may also be blocked across our network as spam. Thank you for your understanding and cooperation.