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Clinical Research Technician 1
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The Clinical Research Technician’s (CRT) role is to assist the study investigator in the performance of specific clinical trial activities as identified on the trial Delegation of Responsibilities Log. The CRT adheres to GCP/ICH, as well as PRA and/ or Sponsor Standard Operating Procedures (SOPs). Responsibilities include but are not limited to obtaining written informed consent, executing clinical trial procedures, performing data analysis, conducting instrument function verification, and facilitating subject flow.


  • Has limited knowledge of the therapeutic area.
  • Applies knowledge of PRA’s and sponsor policies and procedures
  • Good written and oral communication.


  • Read, write, and speak fluent English; fluent in host country language required
  • Minimum one year experience working in Optometry/ Ophthalmology or similar area.

  • BS degree 

  • Experience in Optometry/ Ophthalmology
  • Associates of Sciences with a medical background
  • Experience in Clinical Research 

PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.


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