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Clinical Research Coordinator

Eclipse Clinical Research
Tucson, AZ Full Time
POSTED ON 3/17/2025
AVAILABLE BEFORE 4/15/2025

Eclipse Clinical Research is looking for a highly motivated a clinical research coordinator, will consider an MA that is a quick learner. Must be extremely detail orientated, dependable, and a team player.

Must be proficient in performing phlebotomy, vital signs and EKGs. Must also be able to complete patient visits according to protocol and recruit patients. Needs reliable transportation as the job does entail traveling to multiple sites. The ability to multi-task and maintain multiple studies is essential.


Essential job functions/duties:

  • Under the direction of the Principal Investigator or sub-investigator, manage the conduct of clinical research activities.
  • Responsible for coordinating and implementing assigned protocols in compliance with FDA CFR, GCP and company SOPs.
  • Collects and records clinical research data, assists in patient assessments, scheduling, maintain study files, study supplies and study medication accountability.
  • Review the inclusion/exclusion criteria and requirements of each protocol with the principal/sub- investigator
  • Responsible for the recruitment and screening of potential participants, which includes chart review of patients and schedules, contacting leads from outside recruitment efforts, and following up on referrals from all sources.
  • Responsible for meeting recruitment goals for each study.
  • Provides informed consent forms and educational information to study participants.
  • Screen and enroll study subjects
  • Manage study-related activities, subject compliance and documentation
  • Ensure compliance with protocol
  • Correct and edit data as directed and as appropriate.
  • Obtaining patient medical history and medication lists
  • Phlebotomy and basic laboratory tests
  • ECG/Vital signs
  • Administer questionnaires and assessments
  • Study drug administration, including injections
  • Tracking inventory and reordering when necessary
  • Other responsibilities as delegated.


Qualifications

  • Clinical Research Coordinator or Medical Assistant experience
  • BLS for healthcare providers certification
  • Experience with EHR systems and medical terminology
  • Ability to perform intake and monitor vital signs accurately
  • Knowledge of phlebotomy procedures


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