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Clinical Research Coordinator

2 months ago

Phoenix, United States Medix™ Full time

We are looking for a well versed Clinical Research Coordinator that is bilingual/fluent in Spanish. The ideal candidate will have a minimum of 2 years of experience as a CRC and have experience with tasks such as EKGs, vitals, & phlebotomy. This position is on-site and a direct hire (permanent).


Responsibilities

  • Perform overall data management of studies — collect, enter, and maintain records for clinical study subjects.
  • Support accurate and timely data entry in electronic databases.
  • Ensure all protocol-required procedures and visits occur according to specified guidelines.
  • Manage participant enrollment and ensure compliance with the protocol during participant recruitment, informed consent, participant education, eligibility assessment, participant care, and follow-up per protocol.
  • Collaborates with quality assurance (QA) in the development of source documentation for new studies, assisting in the assessment of toxicities/adverse events and reporting serious adverse events per IRB and sponsor requirements.
  • Possess excellent interpersonal skills and collaborative with the research team.
  • Independently manage workflows and prioritize numerous tasks.
  • Be flexible and anticipate timeframes to accommodate frames subjects, monitors, and overtime hours during high-enrolling study periods.
  • Maintains GCP certification and IATA training as required.
  • Performs other duties as assigned.


Requirements

  • At least two years of experience as a clinical research coordinator.
  • Experience with Phlebotomy
  • Excellent oral and written communication skills.
  • Demonstrated ability to work well independently and with subordinates.
  • Demonstrated ability to manage frequent deadlines and competing priorities.
  • Computer proficiency.
  • Critical thinking and analytical skills