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2017-42896

2017-42896

Title 
Senior IxRS UAT Specialist
Job Locations 
-
US-Remote
Posted Date 
11/17/2017

More information about this job

Overview

The IxRS UAT Specialist uses technical, industry and interpersonal skills to develop and oversee the execution of User Acceptance Testing (UAT) Plans for IxRS. This includes but is not limited to performing quality reviews of the User Requirements Specification and User Acceptance Testing deliverables, following the UAT process and training testers and other PRA staff in UAT execution.

Responsibilities

  • Ability to function as Study Matter Expert on UAT for Clinical Teams
  • Responsible for writing the end-to-end Interactive Voice/Web Response System UAT Plan
  • Providing peer review and comments for UAT Plans created by Peers
  • Responsible for quality review of the URS, UAT Requirements and UAT deliverables
  • Support CIM in UAT Coordination, UAT execution and UAT error resolution
  • Ability to lead meetings with internal and external stakeholders to present UAT material
  • Ability to guide/instruct participants during the execution of UAT
  • Ability to manage multiple projects/timelines
  • Collaborate with both Sponsor external vendors and internal functions to develop scenarios for testing purposes.
  • Work within published study/system project timelines and attend meetings as necessary
  • Conform with GMP and GDP practices
  • Assist in training and mentoring junior levels
  • Participate in or lead PRA initiatives as directed by functional management
  • Ability to create UAT plans from User Requirements Specification (URS)
  • Interprets URS and clinical study protocols
  • Familiarity with the Software Development Life Cycle (S DLC): reviewing requirements, Testing, Documentation, and Deployment.
  • Applies knowledge of PRA’s SOPs, Work Instructions and related guidance, and of the pharmaceutical or CRO industry.

Qualifications

  • Bachelor's degree required. 
  • Minimum 4 years Prior Interactive Voice/Web Response System (IVRS and IWRS) experience in a clinical supply chain management environment.
  • Experience overseeing projects including team members and timelines.
  • Prior clinical trials experience.
  • Experience writing test scripts is highly desired.
  • UAT testing experience is required.
  • To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status.

 

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

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