Site CRC 1 - UT in Salt Lake City, UT at Apex Life Sciences

Date Posted: 2/28/2018

Job Snapshot

  • Employee Type:
  • Job Type:
  • Experience:
    At least 1 year(s)
  • Date Posted:
  • Job ID:

Job Description


  • To work as an integral member of partner/investigator site staff maintaining the day-to-day relationship with a partner site/s involving planning, coordinating and, as appropriate, execution of clinical studies in accordance with the protocol, contracted scope of work, ICH/GCP, Sponsor SOP's and any relevant local guidelines and regulations.


  • Work directly at patient/subject interface at investigator sites to deliver high quality patient data in accordance with local regulations, agreed scope of work and as required by protocol.
  • Assist with screening and enrollment of subjects into an in depth Schizophrenia clinical trial.
  • Support subjects on trials to encourage maximum retention and future recruitment.
  • Assist with the establishment of a recruitment and contingency plan for each study.
  • Perform functions necessary for successful completion of all protocol required visits/procedures such as vital signs, phlebotomy, diagnostic tests, dispensing of investigational product, scheduling, drug accountability/reconciliation and organizational tasks, where appropriate and as delegated by the investigator, in accordance with local country requirements.
  • Accurately complete source documents and case report forms in both paper and electronic format.
  • Assist investigator with recording and reporting of adverse events as per local regulatory authority guidelines.
  • Perform other duties as assigned per protocol and / or investigator.


  • Good knowledge of medical terminology.
  • Above average interpersonal and organizational skills.
  • Proficient in the use of Microsoft Office.
  • Fluent in local language, spoken and written.
  • Fluent in written English language.
  • Ability to work independently, prioritize actively, seek input, problem solve and work in a team environment.
  • Ability to maintain confidentiality.
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients.


  • Registered nurse, medical physician or appropriate educational qualification and minimum 1 years' experience being a Clinical Research Coordinator.
  • Experience in Schizophrenia or Psychology based clinical studies is a strong preference.

Please email: for consideration.