Clinical Research Coordinator I / Data-Entry

Arizona Liver Health•Tucson, AZ

2d•$23 - $27•Onsite

About The Position

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. Title: Clinical Research Coordinator I (Data Entry) Compensation: $23 to $27 per hour, depending on experience Location: Tucson, AZ Schedule: Monday-Friday, Onsite, 7am-4pm Essential job functions/duties Reasonable accommodation may be made to enable individuals with disabilities to perform these essential functions. File documents in the binder (I.e., subject source, labs) Enter clinical research data into appropriate fields. Transfer data from paper formats via computer, recorders, or scanners EDC entry Review and edit data to ensure completeness and accuracy of information; follow up with subjects to resolve problems or clarify data collected. Answer Queries Curate data directly from clinical research Analyze statistical and graphical Data. Prepare documents and charts for subject visits. Assist patients with surveys Obtain and print procedural/imaging reports for review by the investigator Print labs and prepare for Investigator to review File lab results to subject binder or where required Ensure W-9 and medical release forms are signed by subjects annually Prepare correspondence, documentation, or presentation materials on findings Assist with the management of study supplies and order resupply Perform miscellaneous job-related duties as assigned Request medical records prior to visit and print for filing as needed Plan, schedule, and confirm of subject research visits as needed Update CTMS as needed Maintain training as needed including but not limited to GCP, IATA, EDC, Protocol training, Delegation of Authority and others as required Ability to interact and communicate with clarity, tact and courtesy with patients, staff, faculty and others Develops strong working relationships and maintains effective communication with study team members Complies with ALH, clinic and sponsor policies, standard operating procedures (SOPs) and guidelines Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines Additional duties to be assigned to role as applicable Conduct Clinical Research study visits when assigned 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

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
0-2 years of experience in the field or in a related area
Must have valid documentation and authorization to work in the U.S.

Nice To Haves

Associate degree preferred.

Responsibilities

File documents in the binder (I.e., subject source, labs)
Enter clinical research data into appropriate fields.
Transfer data from paper formats via computer, recorders, or scanners
EDC entry
Review and edit data to ensure completeness and accuracy of information; follow up with subjects to resolve problems or clarify data collected.
Answer Queries
Curate data directly from clinical research
Analyze statistical and graphical Data.
Prepare documents and charts for subject visits.
Assist patients with surveys
Obtain and print procedural/imaging reports for review by the investigator
Print labs and prepare for Investigator to review
File lab results to subject binder or where required
Ensure W-9 and medical release forms are signed by subjects annually
Prepare correspondence, documentation, or presentation materials on findings
Assist with the management of study supplies and order resupply
Perform miscellaneous job-related duties as assigned
Request medical records prior to visit and print for filing as needed
Plan, schedule, and confirm of subject research visits as needed
Update CTMS as needed
Maintain training as needed including but not limited to GCP, IATA, EDC, Protocol training, Delegation of Authority and others as required
Ability to interact and communicate with clarity, tact and courtesy with patients, staff, faculty and others
Develops strong working relationships and maintains effective communication with study team members
Complies with ALH, clinic and sponsor policies, standard operating procedures (SOPs) and guidelines
Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
Additional duties to be assigned to role as applicable
Conduct Clinical Research study visits when assigned
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