Covance

  • Proj Mgr IV

    Job Location(s) UK-Maidenhead | BE-Brussels | NL-Amsterdam | DE-Munich | FR-Paris | IT-Milan | IT-Rome | ES-Barcelona | ES-Madrid | PT-Lisbon | CZ-Prague | ...
    Job Number
    2019-26882
    Job Category
    Project Management
    Position Type
    Full-Time
  • Job Overview

    The Project Manager is responsible for the day−to−day cross−functional operations of the assigned study or studies for one or more clients. As the team leader, the Senior Project Manager will ensure assigned studies are delivered successfully, on−time, within budget, according to client expectations and with the highest level of quality possible. The Senior Project Manager may manage any combination of the following: single or limited services study or a small regional cross−functional study. Furthermore, a Senior Project Manager may also manage a portion of a larger global study within a given geographical region (i.e. North America, Western Europe, etc.)

     

    Duties & Responsibilities

     

    • Manage, lead and motivate cross-functional project teams, facilitating the team’s ability to complete their responsibilities in accordance with project contracts, contract amendments, applicable regulatory, GCP and SOP requirements as well as company policies and procedures
    • You shall function as the primary liaison between client, third party vendors and the Chiltern project team for project issues
    • Developing and maintaining project metrics, timelines, budget and deliverables including project plans, trackers and tools for assigned projects
    • You must proactively manage project budgets, including scope and scope changes, costs, forecasts and margin evaluations
    • Manage day-to-day operational aspects of assigned projects including third party vendor activities

    Education / Qualifications

    • A successfully completed university degree preferably in science, nursing or applicable industry-related experience

    Experience

    • Candidates must have Medical Device Project Management experience working in a CRO setting.
    • Working knowledge of local regulatory requirements and GCP/ICH guidelines or ISO guidelines
    • Demonstrate good presentation skills
    • Proficiency in Microsoft Office and familiarity with standard project management tools/applications
    • Fluent in English and local language (written & spoken)

     

    THERAPEUTIC FOCUS:

     

    Experience in Device/Cardiac-Device is needed.

     

    Additional information:

    • Office or home based as appropriate
    • 20% travel availability nationally and potentially internationally clients, attendance at conferences and presentations
    • No freelance applications or agency enquiries will be considered

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