Clinical Research Coordinator I (CRC1) Flagstaff
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. Arizona Liver Health/Arizona Clinical Trials is looking for qualified candidates for the Clinical Research Coordinator I position in Flagstaff.
Requirements
- High School Diploma or GED required
- 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
- 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
- Demonstrated excellent organizational skills.
- Demonstrated experience working as part of a team.
- Relevant subject matter knowledge.
Nice To Haves
- Associate Degree or Bachelors degree is preferred
- Bilingual - Spanish preferred
- Vaccine trial experience 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
- 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
- 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
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 company match
- Short & Long Term Disability
- Educational Assistance
- Shared company vehicles for required travel
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
