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Clinical Research Associate 3
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The Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.


Same as level 1 & 2
  • If responsible for supervising other CRAs: Schedules and reviews trial tasks, provides leadership in the delivery of services to clients, ensures that staff fulfill their responsibilities in accordance with PRA’s policies, procedures, and SOPs, and ensures HR processes are properly implemented
  • Serves as a Preceptor for new CRAs participating in the CRA Bridge Program
  • Functions independently with minimal oversight required
  • May serve as subject matter expert for  CTM on monitoring related activities
  • May be assigned to complex studies and/or sites
  • Provides leadership skills to assigned projects and within the Clinical Operations department


  • Read, write and speak fluent English; fluent in host country language required.
  • Knowledge of ICH and local regulatory authority regulations regarding drug
  • 5+ years of clinical monitoring experience required

  • Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience required

  • Clinical research experience
  • Knowledge of ICH and local regulatory authority regulations regarding drug
  • An advanced degree (e.g., M.S., M.B.A., PharmD, etc)
  • Experience in monitoring complex trials
  • Participation in departmental initiatives

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


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