Clinical Research Coordinator II
Premier Research - Phoenix, AZ

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Coordinates and conducts research protocols in a manner that ensures quality, consistency, timeliness, accuracy and patient safety.

Establishes and maintains frequent face-to-face, written and telephone contact with various persons involved in the study, including but not limited to the subjects, relatives/friends of the subjects, doctors, pharmaceutical sponsors, pharmacists and all levels of Research Centers staff

Functions in the role of Lead or co-lead on studies as assigned, some of which may be complex

Identifies, evaluates and recruits qualified potential subjects for the clinical research study assigned

Becomes thoroughly familiar with the regulatory documents, protocol, case report form, informed consent, source documentation, subject 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, including completion of minutes and follow-up reports

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

Dispenses appropriate investigational medication to each study participant per protocol instructions

Provides Project managers with summary data related to all study activities

Is responsible for high level administrative study oversight

May aid in the development of Clinical Assistant and Clinical Coordinator l staff

All other projects as assigned

Required Skills

Key Skills:
Excellent communication skills (interpersonal, written, verbal)

Strong attention to detail

Excellent time management and organizational skills

Intermediate computer skills

Current Paramedic or LVN license, with a minimum of two years direct clinical research with at least one year experience coordinating research studies

Current EMT-B with two years direct experience coordinating more complex research projects

Equivalent: Bachelor’s Degree in Health Science, with a minimum of two years direct clinical research experience, at least two of which were in more complex projects

Equivalent: Minimum of three years direct clinical research experience,

Education or Certification:
CPR Certification preferred

CRC Certification preferred

Phlebotomy certification (national) preferred

Required Experience

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