Clinical Research Coordinator I (PRN Phone Screener)
Premier Research - Austin, TX

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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.
  • Function in the role of lead or co-lead on studies as assigned
  • Identifies, evaluates and recruits qualified potential subjects for the clinical research study assigned
  • 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
  • Distributes copies of protocol to study staff, including investigators
  • 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, 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
  • All other projects as assigned
Required Skills
  • Bachelors degree in Health Science or equivalent
  • CPR Certification
  • Phlebotomy certification (national) preferred
  • Maintain current status of nursing license or paramedic certification (if applicable)
  • Current LVN license or paramedic certification OR Bachelors degree in Health Science and a minimum of one year direct clinical research experience OR Capable of preparing for CRC certification
  • Excellent communication skills (interpersonal, written, verbal)
  • Strong attention to detail
  • Excellent time management and organizational skills
  • Basic computer skills
Required Experience
  • Minimum 3 years as a Clinical Assistant

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