Covance

  • eCOA Validation Lead

    Job Location(s) US-NC-Raleigh-Durham | US-PA-Philadelphia | US-TX-Austin | US-PA-King of Prussia | US-NJ-Princeton | US-IL-Chicago | US-MO-Kansas City | CA-ON-Toronto | CA-ON-Mississuaga
    Job Number
    2018-23791
    Job Category
    Other
    Position Type
    Full-Time
  • Job Overview

    eCOA Validation Lead

     

    Permanent, salaried

    Remote from anywhere in the U.S. or Canada

     

    Responsibilities

    • Proactively follow-up with customers and third-party vendors to ensure comprehensive understanding of requirements and design in order to provide quality deliverables.
    • Active participation in study team meetings.
    • Review and provide input on requirements and specifications.
    • Create validation documentation – UAT Test Plan, test scripts, and defect tracker.
    • Direct teams during testing execution for initial implementation and updates. Function as point of contact during UAT for team members, triaging and resolving issues as needed.
    • Manage UAT plans and timelines, ensuring that team members adhere to the schedules and timetables for the completion of projects.
    • Advise the team and stakeholders, informing on the processes that will be completed to enable system implementation.

     

    Education/Qualification

    • Degree in a mathematical, computing, life sciences, or related discipline

     

    Experience

    • Minimum 2-4+ years of experience in clinical systems such as CTMS, ePRO, IXRS, EDC or an equivalent combination of education and experience to successfully perform the key responsibilities of the job
    • Strong oral and written communication skills. Experienced project leader and presenter.
    • Proficiency in converting complex technical and business requirements into clear test plan and test cases.
    • Understanding of Drug Development and Clinical Trial Processes
    • Understanding of Data Management Processes
    • In-depth knowledge of Good Clinical Practices
    • Understanding of Clinical Research System Development Lifecycle
    • Must have sound problem resolution, judgment and decision-making skills.
    • Ability to prioritize tasks effectively and manage multiple projects simultaneously.

    Education/Qualifications

    Education/Qualification

    • Degree in a mathematical, computing, life sciences, or related discipline

    Experience

    Experience

    • Minimum 2-4+ years of experience in clinical systems such as CTMS, ePRO, IXRS, EDC or an equivalent combination of education and experience to successfully perform the key responsibilities of the job
    • Strong oral and written communication skills. Experienced project leader and presenter.
    • Proficiency in converting complex technical and business requirements into clear test plan and test cases.
    • Understanding of Drug Development and Clinical Trial Processes
    • Understanding of Data Management Processes
    • In-depth knowledge of Good Clinical Practices
    • Understanding of Clinical Research System Development Lifecycle
    • Must have sound problem resolution, judgment and decision-making skills.
    • Ability to prioritize tasks effectively and manage multiple projects simultaneously.

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