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Job Details


Labcorp (Drug Development)

IRT Test Lead

Pharmaceuticals

All

Full Time

On Site

No

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.

Experience:
  • 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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