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  • Posted: Apr 28, 2022
    Deadline: Not specified
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    Sharing a Vision to Drive Healthcare Forward Healthcare is an industry designed to help humans. As a global community, we continuously invest and commit to advancing human health. To deliver value and real outcomes. To rise to the challenge to find the next breakthrough by making the most of increasingly limited resources. We are inspired by the potential ...
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    Clinical Project Manager, Real World Evidence (Home-Based, flexible across Europe)

    Responsibilities:

    Through your management of clinical project teams, you’ll be responsible for global clinical study and project productivity, delivery and quality, resulting in strong financial performance and most importantly, customer satisfaction.

    You’ll participate in bid defence preparations, and, in the Senior Clinical Project Manager role, will have the opportunity to lead bid defence presentations in partnership with our Business Development teams for multi-country/region studies. You’ll also be involved in developing the delivery strategy for RFP’s.

    Other responsibilities, depending on the level of the role may include:

    • Managing and co-ordinating efforts of cross-functional project teams to support milestone achievement and to manage study issues and obstacles. Implementing continuous improvement activities for assigned projects
    • Serving as primary project contact with Sponsor to ensure communication is maintained and continuously improved and reporting schedules are adhered to
    • Reporting on team performance against contract, customer expectations, and project baselines to management
    • Leading problem solving and resolution efforts to include management of risk, contingencies and issues. Developing proactive contingency plans to mitigate clinical risk
    • Providing input to line managers of their project team members' performance relative to project tasks and supporting staff development
    • Support less experienced CPMs
    • Ensure high performance and efficiency of the clinical team through the scheduling of co-monitoring/accompanied site visits and ongoing mentoring of CRA team
    • Prepare and present project information at internal and external meetings

    Candidate Requirements:

    • You must have previous experience managing international clinical studies in Late Phase prospective and retrospective activity including Non-Interventional/Observational Studies in the CRO/pharmaceutical industry.

    For both roles you’ll also need:

    • Strong collaboration and influencing skills, with experience of managing cross-functional project teams
    • Proven ability to work independently in a complex matrix environment
    • Thorough knowledge of GCP and global clinical development processes
    • Demonstrable presentation, diplomacy, negotiation and conflict resolution skills
    • A strong customer-oriented mindset
    • Already possess the right to work in the hiring country without the need of a visa/sponsorship

    And in addition for the Senior CPM role:

    • Bid defense experience
    • 2 further years experience as detailed above
    • Study budget management experience
    • Proven ability to coach and mentor

    Method of Application

    Interested and qualified? Go to IQVIA on jobs.iqvia.com to apply

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