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  • Posted: Oct 29, 2020
    Deadline: Not specified
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    The story of PRA Health Sciences would naturally talk about how we’ve become one of the world’s largest CROs. It would talk about our innovation and growth and would speak to our operational efficiencies and transparency. It would highlight our expertise and customization. And it would touch on the incredible differences we’ve made, over ou...
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    Clinical Project Manager

    The Role

    Working as the leader of a cross-functional study team and for a mix of sponsors, our Project Managers are at the forefront of this success. From the bid defense onwards, you will lead a team of other internal study team members with a high focus on quality to ensure successful delivery to our clients.

    A significant part of your work will be to build and manage the study budget, implement actions to mitigate areas of risk, drive delivery across the full project, collaborate with internal stakeholders to track study progress and create study tools. Naturally, as a Project Manager, you will also be instrumental in the management of the client via close collaboration, both in person and remotely

    Responsibilities:

    • Responsible for successful execution of projects in line with project specifications: timelines, budget, quality and resources - Key tasks include leading the project team, finalization of project plans including training plans, tracking of project metrics and KPIs
    • Overall responsibility for the performance and progress of each functional area (Clinical, Data, Stats, Drug Safety, Medical, Regulatory)
    • Primary contact for client ensuring their objectives and expectations are understood and managed; experience with a range of customers from small Biotech as well as leading Pharmaceutical firms
    • Project financial control and liaison with finance, contracts and billing team to ensure adherence to contract, budget and invoicing requirements
    • Management of third party vendors: strategic partners, central laboratories, central imaging, randomization systems, drug depots, training vendors
    • Investigator Meeting planning and experience working with KOLs and Steering Committees to build consensus on trial design and plans as well as publication planning
    • Involved in bids to win new project work

    You are:

    Innovative, forward-thinking and delivery-focused. Here at PRA we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have:

    • A proven track record as a highly motivated and dynamic project management professional
    • Experience of leading full service, multi-country clinical studies
    • Sponsor and budget management
    • A strong commercial knowledge of the pharmaceutical industry
    • Previous proven success in working in a CRO environment
    • Excellent communication skills
    • The ability to build strong external relationships and motivate a regional or global team

    Your health, your family, your career, your money — the things that matter to you, matter to us. The benefits of PRA just get better and better.

    Method of Application

    Interested and qualified? Go to PRA Health Sciences on prahs.com to apply

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