Sr Clinical Research Coordinator (CRC)
Premier Research - Phoenix, AZ

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Sr Clinical Research Coordinator (CRC)

Research Centers

Responsible for managing assigned clinical research projects, including oversight and training of project personnel.

  • Establishes and maintains frequent face-to-face, written and telephone contact with various persons involved in the study, including but not limited to the patients, relatives/friends of the patients, doctors, pharmaceutical sponsors, pharmacists and all levels of Research Centers staff.
  • Ensures potential subjects/patients for the clinical research study are identified, evaluated and recruited.
  • Becomes thoroughly familiar with the protocol, case report form, informed consent, source documentation, patient diary (when applicable), and study medication(s) for the assigned research study
  • Coordinates and conducts pre-study, initiation, monitoring and close-out visits with the pharmaceutical representative. Includes completion of minutes and follow-up reports
  • Coordinates multiple studies simultaneously as required
  • Performs appropriate research protocol procedures which may include, but are not limited to: vital signs, pregnancy tests, intravenous catheter insertion (if license permits), blood collection and processing, ECGs, alcohol breath tests and pain assessments
  • Performs basic lab procedures, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-ups
  • Aids in the coordination of external or off-site studies
  • Monitors, records and is prepared to provide medical care as needed
  • Provides Project managers with summary data related to all study activities
  • Participates in the professional development of other clinic personnel by providing one on one mentoring and in-services

Key Skills:
  • Excellent communication skills (interpersonal, written, verbal)
  • Strong attention to detail
  • Excellent time management skills
  • Intermediate computer skills
  • Current LVN or Paramedic license, with a minimum of three years direct experience coordinating multi-level projects
  • Equivalent
  • : Bachelor’s Degree in Health Science, with a minimum of three years direct clinical research experience, at least two of which were in multi-level projects Equivalent: Minimum of four years direct clinical research experience, at least three of which were in multi-level projects

Education (Degree) or certifications:
  • CPR Certification (preferred)
  • CRC Certification (preferred)
  • ACLS Certification (preferred)

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