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ePRO Specialist
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Provide end-to-end support to the ePRO startup, conduct, and closeout activities for clinical studies.


  • Perform ePRO related activities including, but not limited to: 
    • kickoff ePRO development
    • draft/finalize user requirement specification
    • participate in the UAT execution
    • manage ePRO project schedule
  • Coordinate resolution & risk mitigation of all ePRO related issues and end of study vendor deliverables
  • Write / update standard operating procedures, develop a library of ePRO data capture and reporting standards, as needed
  • Provide support to the IVRS team in the capacity of IVRS coordinator, as needed.
  • Establish Project Plan using Microsoft Project
  • Work with Vendor PMs to maintain timelines and determine resources
  • Participate and execute UAT scripts/Change Requests
  • Ensure sites/patients have device inventory
  • Support database lock activities
  • Write SOPs and Job Aids
  • Serve as ePRO Subject Matter Expert


  • Bachelor's degree in Computer Science, Biology or related discipline preferred
  • Minimum 3 years experience in clinical data management preferred
  • Solid experience in study startup activities for EDC InForm / ePRO
  • Past ePRO startup, conduct, and closeout experience

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


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