Clinical Research Coordinator I (Phase I) (Sat.-Sun.)

Arizona Liver Health•Chandler, AZ

4h•$25 - $30•Onsite

About The Position

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. Title: Clinical Research Coordinator I (Phase I) Compensation: $25 to $30 per hour, depending on experience Location: Chandler, AZ (AMP) Schedule: Part-time (24 hours), Saturday-Sunday, 7am-7pm Essential job functions/duties Reasonable accommodation may be made to enable individuals with disabilities to perform these essential functions.

Requirements

Knowledge of commonly used concepts, practices, and procedures in Research field.
Strong attention to detail.
Excellent communication skills.
High School Diploma or GED required.
BLS and ACLS training required.
1-2 years of experience in Clinical Research, Medical Assistant, Phlebotomy, or Medical Scribe
Must have valid documentation and authorization to work in the U.S.

Nice To Haves

Bachelor’s degree preferred.
Medical Assistant certification or diploma from an accredited program preferred.
Professional certification in phlebotomy from a recognized program preferred.

Responsibilities

Conduct study required procedures within study specific guidelines/timeline and document in real time.
After proper training and delegation will be required to perform all study related procedures required on their shift and in preparation for the next shift. The procedures may include performing ecgs, vital signs, administering subject home medication, administering IP (Investigational Product/study drug) under direction of pharmacy staff, administer questionnaires as required per protocol, start iv’s after, draw and process blood per lab manual, urine collection, keep intake and output sheets, collect and process bodily secretions per study guidelines. Other duties as assigned to keep in compliance with protocol requirements and data collection.
Subject education and training as required.
Answer phone calls and direct appropriately.
Order subject meals and ensure they eat per protocol requirements. Ensure subject and staff meals are within company guidelines.
Training in BLS/ACLS per company policy. Call 911 if emergency situation arises and notify investigator immediately.
Notify investigator or other delegated staff of any changes in subject status or reports of complaints by subject.
Administer over-the-counter medication under direction of investigator.
Assist subject with hygiene needs as required. Keep rooms clean and change bed linen as needed.
Take subjects on walks outside and attend during smoking breaks.
Keep stock of snacks, sodas, water, etc. Order or provide list of needed supplies to Phase 1 staff member.
Keep drawers, closets stocked with needed supplies.
Monitor visitors and clinic visitation hours.
Document all adverse events as required per protocol. Investigator and/or clinical coordinator should be notified in a timely manner of any potential adverse reactions.
If new subjects check in to the unit during your shift, ensure all bags are checked for prohibited items. If these items are found, they should be confiscated and locked in a secure area for the safety of all subjects and staff. This will include cigarettes and lighters, pocket knives, subject home meds, etc.
Perform all duties according to established policies, procedures, regulatory requirements, as well as applicable professional standards.
File documents in the binder (I.e., subject source, labs)
Enter clinical research data into appropriate fields.
Transfer data from paper formats or electric data via computer, recorders, or scanners.
Review and edit data to ensure completeness and accuracy of information; follow up with subjects to resolve problems or clarify data collected.
Assist with research trial audits.
Prepare documents and charts for subject visits.
Prepare correspondence, documentation, or presentation materials on findings.