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  • Posted: Jan 15, 2021
    Deadline: Not specified
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    As the drug development business of Laboratory Corporation of America Holdings (LabCorp) and the world’s most comprehensive drug development service company, we have helped pharmaceutical and biotech companies develop 49 of the top 50 prescription drugs in the marketplace today. Because of our broad experience and specialized expertise, we’re in ...
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    Project Manager, Start-up

    About the department: This department provides an quality-focused approach to the study start-up phase of site activations with an emphasis on flexibility, collaboration, and efficiency. Our SUPMs oversee and manage multi-functional teams in order to deliver on time Ready to Enrol milestones for our clients. This is an excellent client facing opportunity to develop your career, communications and soft skills, as well take on more responsibilities and be involved in cutting edge global studies.

    Responsibilities

    Expert in, project start-up and related maintenance activities for a particular study/studies on a regional and/or global level as well as excellent communication skills to support client relationships. Responsible for leading, ensuring and overseeing, start-up and/or maintenance activities on projects, on time, within budget, and in compliance with SOPs and/or other quality and regulatory requirements. Depending on the scope of the project and experience level, job duties may be performed independently as a Lead SUPM or in collaboration with a Lead SUPM as a Regional SUPM.

    Education/Qualifications

    Education/Qualifications:

    • University/college degree (life science preferred) or certification in a related allied health profession (i.e. nursing, medical or laboratory technology) from an appropriately accredited institution.
    • Working knowledge of financial control procedures (e.g. costing systems, time reporting).
    • Working knowledge of project management processes, especially regarding study start-up.
    • Working knowledge of time and cost estimate development.
    • Working knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs.
    • Broad knowledge of drug development process and client needs.

    Method of Application

    Interested and qualified? Go to Covance on careers.covance.com to apply

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