Arizona Liver Health · 2 days ago
Clinical Research Coordinator I (Phase I)
Arizona Liver Health (ALH) is dedicated to driving high standards of care and advancing medical innovation through leading clinical trials. The Clinical Research Coordinator I will conduct study procedures, ensure compliance with protocols, and assist in patient care and data management.
Clinical TrialsHealth CareHospitalityMedical
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
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
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
Qualification
Required
High School Diploma or GED required
BLS and ACLS training required
Knowledge of commonly used concepts, practices, and procedures in Research field
Strong attention to detail
Excellent communication skills
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. -- visa sponsorship or transfer is not offered now or in the future
Preferred
Bachelor's degree preferred
Medical Assistant certification or diploma from an accredited program preferred
Professional certification in phlebotomy from a recognized program preferred
Benefits
Health, Dental, Vision (with HSA plans and employer contribution)
2 weeks PTO
5 days Sick Time
7 Company holidays + 2 Half-days
401K with up to 6% company match
Short & Long Term Disability
Educational Assistance
Shared company vehicles for required travel
Company
Arizona Liver Health
Arizona Liver Health provides specialized diagnostics, evaluation, treatment for patients with liver disease and other liver conditions.
Funding
Current Stage
Growth StageLeadership Team
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