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 Clinical Research Coordinator I position in Tucson.

Compensation:
Full-time $21-$25 per hour, depending on experience

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
Serve as back up for pharmacy and lab
Curate data directly from clinical research
Analyze statistical and graphical Data.
Conduct clinical research study visits when assigned.
Audit research trials
Prepare documents and charts for subject visits.
Assist patients with surveys
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
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
Conduct clinical research study visits when assigned
Audit research trials
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

Education & Experience:

High School Diploma or GED required
Associate Degree or Bachelors degree preferred
0-3 years of experience in the field or in a related area
At least 1 year of clinical research experience as a clinical research coordinator and experience working in a medical center or private practice is strongly preferred
Experience using CTMS system and EDC program

Knowledge, Skills, Abilities:

Excellent communication and problem-solving skills
Ability to work effectively with a lead study coordinator on multiple assignments, in a fast paced, multi-tasked environment, exercising sound judgment in setting priorities with a strong attention to detail
Bilingual - Spanish preferred
Demonstrated ability to multi-task.
Demonstrated excellent organizational skills.
Ability to communicate effectively both orally and in writing.
Demonstrated experience working as part of a team.
Relevant subject matter knowledge.

Travel requirements:

Some interoffice travel may be required with use of company vehicle or mileage reimbursement

Benefits & Perks:

Health, Dental, Vision (with HSA plans and employer contribution)
2 weeks PTO
5 days Sick Time
7 Company holidays + 2 Half-days
401K with company match
Short & Long Term Disability
Educational Assistance
Shared company vehicles for required travel

Our company requires COVID-19 vaccinations for all current and future employees. Exemptions can be requested for those with a reasonable health or a religious/sincerely-held belief accommodation.

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.

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.

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Are you a current OR previous employee at AZ Liver Health, AZ Clinical Trials, or VEN Centers? *

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Clinical Research Coordinator I (CRC1)

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