PRAHS

  • Trial Manager (GTM)- Madrid

    Job Locations - | Spain-Madrid
    Posted Date 1 week ago(4/13/2018 4:46 AM)
    ID
    2018-46262
  • Overview

    Providing innovative solutions for our clients is what we do. But innovation just for the sake of innovation isn’t why we do it. Side-by-side with our clients, we strive to move drug discovery forward, to help them develop life-saving and life-improving drugs. We help change people’s lives for the better every single day. It’s who we are. And it’s who you could be too.

     

    Working fully embedded within one of our pharmaceutical clients, with the support of PRA right behind you, you’ll be at the heart of our client’s innovation.

     

    We are looking for a Trial Manager in Madrid to work fully assigned to sponsor.

     

    As a Trial Manager, you will be dedicated to one of our global pharmaceutical clients, a company that values performance, recognises merit and has a high focus on quality. This environment encourages innovation, individuality and embraces people that want to be a part of it.

     

    Responsibilities

     

    The overall purpose of this role is to expertly coordinate global trial activities for internally and/or outsourced trials. For this particular opportunity, the focus will be on project managing local late phase studies (phase IV and observational).

     

    Working throughout the full lifecycle of the trial, you will lead a study team through the feasibility and site selection process, trial set-up, study execution and trial closure.

     

    Key responsibilities will include:

     

    • To set-up vendor activities
    • To ensure study reporting is accurate in real-time
    • To drive issue resolution
    • To manage documentation and issue escalation
    • To establish the process of data collection and drive the site-selection process
    • To determine and communicate country budgets for each country, monitor actual v forecast and manage vendor budgets, providing various updates and tracking spend according to plan
    • To develop study-specific documents including monitoring guidelines, master ICFs, IMP related documentation and feasibility documents. Additionally, you will provide input to cross-functional documents such as safety-related documents and filing and archiving plans
    • To ensure that trial-specific training materials are created and available
    • To set-up and coordinate investigator meetings
    • To serve as the primary contact person for local teams across the globe, managing internal stakeholder relationships and sharing expert knowledge on the study and therapeutic area
    • To set the standard for quality with your study team; ensuring compliance with applicable regulations, internal operating procedures and processes in order that your study management team are ready for any inspection

    Qualifications

    You are:

     

    An experienced project leader, a strong communicator and solution-oriented.

     

    To ensure success within this role, the following are required:

     

    • A proven track record within study management, including experience in developing study-specific documents 
    • An ability to combine creativity, leadership and experience to empower a team to succeed
    • Financial acumen
    • A BA or BSc degree in a health or science related discipline, or be a registered healthcare professional
    • Fluency in English
    • The ability to travel to the local client office as required

     

     

    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.

     

    PRA Health Sciences is an Equal Opportunity Employer. We welcome and encourage diversity in the workplace.

     

    For more information please visit our website: www.prahs.com

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