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Job Details

Labcorp (Drug Development)

IRT Test Lead



Full Time

On Site


Durham, North Carolina, United States

The IRT Test Lead is Responsible for developing and coordinating the end-to-end Interactive Voice/Web Response System User Acceptance Testing.

What to Expect
  • Proactive follow-up with Sponsor and Third Party Vendor to ensure comprehensive understanding of study design and technology design with a view of providing quality deliverables.
  • Responsible for the quality review of UAT deliverables.
  • Active participation in study team meetings.
  • Lead meetings with stakeholders to present UAT material.
  • Manage UAT plans and timelines, ensuring that team members adhere to the schedules and timetables for the completion of projects.
  • Develop UAT documentation consisting of: test cases, scenario based summaries and all other required documents.
  • Main contact with sponsor and all team members for UAT execution and UAT error resolution.
  • Ability to guide/instruct participants during the execution of User Acceptance Testing (UAT) and system integration testing.
  • Collaborate with both Sponsor external vendors and internal functions to develop scenarios for testing purposes.
  • Execute Quality Control related activities.
  • Address and resolve UAT findings with vendor and core teams.
  • Work within published study/system project timelines and attend meetings as necessary.
  • Conform with GMP and GDP practices.
  • Remote-Based position anywhere in US or Canada

Education / Qualifications
  • University / college degree (life sciences, health sciences, information technology or related subjects preferred).
  • Experience and/or education plus relevant work experience, equating to a bachelor's degree will be accepted in lieu of a bachelor’s degree.
  • Fluent in English, both written and verbal.

  • Minimum 4 years’ experience to include working in IRT system and hands on experience with IRT testing and writing test scripts
  • Demonstrate excellent problem-solving skills, a proactive approach and the ability to make sound decisions.
  • Demonstrated skill in leading teams, by example and mentoring staff.
  • Excellent oral and written communication and presentation skills.
  • Knowledge of clinical trial process and data management, CRF/eCRF Design, CDISC.
  • Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical / biotechnological companies.
  • Demonstrated ability to work in a team environment.
  • Demonstrated ability to handle multiple competing priorities.
  • Proven interpersonal skills.

Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.

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