Research Data Entry/Scheduler (Bilingual)

Arizona Liver Health•Tucson, AZ
•$19 - $27•Onsite

About The Position

Arizona Liver Health/Arizona Clinical Trials is hiring a full-time, non-exempt Research Data Entry/Scheduler in Tucson. The role supports clinical research by processing medical record requests, scheduling research and procedure appointments, coordinating with vendors and on-site monitors, managing subject stipends, and reconciling clinical trial management system data. The position works in a clinic setting and may require some interoffice travel using a company vehicle or mileage reimbursement. Spanish bilingual ability is required.

Requirements

  • High school diploma or GED.
  • Clinical research experience or experience working in a medical center or private practice.
  • Experience using a CTMS system and an EDC program.
  • Bilingual Spanish-speaking ability.
  • Excellent communication and problem-solving skills.
  • Ability to work effectively with a lead study coordinator on multiple assignments in a fast-paced, multitasked environment, set priorities using sound judgment, and maintain strong attention to detail.
  • Understanding of good clinical practice (GCP) and regulatory compliance.
  • Ability to multitask.
  • Excellent organizational skills.
  • Ability to communicate effectively orally and in writing.
  • Relevant subject matter knowledge.

Responsibilities

  • Process medical record requests for study subjects in a timely manner and present records to the Investigator.
  • Schedule necessary procedure and research appointments for study subjects.
  • Liaise with vendors to ensure procedure appointments and medical requests are processed in a timely manner.
  • Coordinate on-site monitor visits and respond to requests within 48 hours.
  • Process subject stipends according to the informed consent form daily and check monthly that stipends have been paid.
  • Communicate professionally with research subjects about stipend or card issues.
  • Reconcile CTMS data daily and monthly, including unsubmitted visits, unpaid stipends, and overdue visits.
  • Audit research trials and file as needed.
  • Adhere to IRB-approved protocols.
  • Comply with institutional policies, standard operating procedures, and guidelines.

Benefits

  • Health, dental, and vision insurance, with HSA plans and employer contribution.
  • Two weeks of PTO.
  • Five days of sick time.
  • Seven company holidays and two company half-days.
  • 401(k) with company match.
  • Short- and long-term disability.
  • Educational assistance.
  • Shared company vehicles for required travel.
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