Research Coordinator

7 days ago


Phoenix, Arizona, United States Common Spirit Full time
Job Summary

We are seeking a highly skilled Clinical Research Coordinator to join our team at Common Spirit. As a Clinical Research Coordinator, you will play a critical role in ensuring the successful conduct of clinical trials and studies.

Key Responsibilities
  • Ensure compliance with regulatory requirements, including FDA, OHRP, and IRB guidelines.
  • Recruit and screen potential participants for clinical trials.
  • Coordinate with investigators to obtain informed consent and enroll participants in studies.
  • Perform various procedures, including laboratory tests, phlebotomy, vital signs, ECG, and outcomes assessments.
  • Obtain medical history and medical records as required by study protocols.
  • Respond to patient inquiries in a timely manner.
  • Process and ship laboratory samples as outlined in study protocols.
  • Provide participant education and training on study procedures, proper dosage, and specific restrictions.
  • Complete case report forms, data entry, and maintain source documentation for all study participants.
  • Prepare for participant visits, including scheduling and source document creation.
  • Triage, track, and report adverse events and deviations to investigators, sponsors, and IRB.
  • Coordinate research monitor visits and respond to data queries in a timely manner.
Requirements
  • Minimum 2 years of related experience required.
  • Competent in computer skills, including Microsoft Office products.
  • Associates degree in a related field or an equivalent combination of relevant education and/or job-related experience in lieu of degree required.
Preferred Qualifications
  • Three (3) years of clinical research experience preferred.
  • Bachelors degree in a related field preferred.


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