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Sr Clinical System Designer
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Uses technical, industrial, and interpersonal skills to create case report forms (CRFs) for trials.


  • Lead and serve as main point of contact relevant to the Clinical Systems group. Responsible for managing timelines and budget. Directly engages with client and internal cross-functional teams.
  • Organizes, creates, and oversees the administration of training and mentoring for junior levels.
  • Helps prepare materials and participate in industry meetings as a representative of PRA.
  • Assists in the development of materials for the bid defense process and client demonstrations.
  • Creates and maintains libraries for use in designing, developing, and testing all system components for a trial.
  • Provides support and review for the re-use of library items.


  • Bachelor’s degree in a technological or clinical field required.
  • Minimum of 5 years of clinical design experience required.
  • Must be RAVE trained/experienced. RAVE certification strongly preferred. Experience with RAVE migrations (documentation and post-migration steps) desired.
  • Experience with integrations with IXRS desired.
  • Prior CRO experience required.
  • Must have prior experience building from the protocol. Must be able to read and understand protocol, and develop new CRFs with minimal support.
  • Must be comfortable interfacing directly with clients and internal cross-functional teams (Lead Data Managers, Developers).

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


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