PRAHS

  • Trial Manager

    Job Locations - | Israel-Tel Aviv
    Posted Date 3 weeks ago(8/1/2018 9:59 AM)
    ID
    2018-48305
  • 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.

    Responsibilities

    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.

     

    Key responsibilities will include:

    • Ensuring study reporting is accurate in real-time
    • Driving issue resolution
    • Managing documentation and issue escalation
    • Establishing the process of data collection and drive the site-selection process
    • Determining and communicating country budgets for each country, monitoring actual v forecast and managing vendor budgets, providing various updates and tracking spend according to plan
    • Accountable for the operational oversight of assigned IISs at an operating company level from start-up (post ReCAP approval) through receipt of the final deliverable and close-out activities and that IISs are conducted in accordance with all applicable regulations/guidelines and applicable Client Policies, SOPs
    • Maintaining communication with the Sponsor-Investigator and staff during all phases of the IIS regarding study progress, issue identification/resolution, contractual matters including payments and collection of required documents
    • Monitoring study progress and initiating corrective and preventative actions when the trial deviates from plans, communicates study progress and issues to IIS team members in support of Medical Affairs/R&D Study Responsible Physician/Study Responsible Scientist
    • Ensuring that contracts, budgets and payment schedules are prepared in accordance with IIS contract requirements and HCC/HCBI consideration
    • Accountable for drug management (e.g. projections, requests) for assigned IIS'
    • Establishing and maintaining excellent working relationships with external stakeholders, in particular investigators, study trial coordinators and other site staff, internal stakeholders, including Medical Affairs and R&D Therapeutic Areas

     

    Qualifications

    You are:

     

    A project leader, a strong communicator and solution-orientated.

     

     

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

     

    • A proven track record within study management at a global level
    • 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 and Hebrew

    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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