Covance

  • Manager of Statistical Programming

    Job Location(s) US-MO-Kansas City | US-Nationwide | CA-ON-Toronto | CA-ON-Mississuaga | US-PA-Philadelphia | US-NJ-Princeton | US-TX-Austin | US-IL-Chicago | US-NC-Raleigh-Durham
    Job Number
    2018-22110
    Job Category
    Biostatistics/Programming
    Position Type
    Full-Time
  • Job Overview

    Manager of Statistical Programming

    This permanent, salaried position can be done remotely from anywhere in the U.S. or Canada.

     

    The selected candidate will be responsible for representing the Biometrics department on interdepartmental project teams and assist in the administration of the department, including resource and project scheduling, interviewing and hiring, establishing departmental processes and interaction with other departments. Additionally, you will also be responsible for the following:

     

    • Supervise, train and conduct performance reviews for staff
    • Work extensively with Biometrics team members and communicate with cross-functional team members
    • Set project priorities and timelines and ensure overall consistency of a project, including macro definitions, debugging programs and documentation
    • Represent Biometrics department on interdepartmental project teams and serve as client contact and primary programmer for clinical trials of various phases
    • Implementing project management methodology
    • Oversee programming of the programmers assigned to project

     

    Education/Qualifications

    • We require a Bachelor’s degree, Master’s preferred or or Higher

    Experience

    • Minimum 5+ years’ experience, or an equivalent combination of education and experience required to successfully perform the key responsibilities of the job
    • Prior experience as a programmer or lead programmer
    • Extensive experience leading statistical programming activities in clinical research
    • Experience leading statistical programming activities for a multiple protocol program preferred
    • Significant previous experience in a pharmaceutical research or CRO setting required

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