• Clinical Project Manager (CPM)- office based Madrid

    Job Locations (All) | Spain-Madrid
    Posted Date 2 weeks ago(1/2/2019 11:34 AM)
  • 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.


    We are looking for a Clinical Project Manager based in Madrid.


    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.


    As a Clinical Project Manager, you will be dedicated to one of our global pharmaceutical clients; a client with which PRA shares a common vision of bringing life-improving drugs to market. 


    We are seeking an experienced Clinical Project Manager to work as an integral part of our pharma client’s global study team. The key function of the Clinical Project Manager is to provide operational country oversight and monitor progress of local activities of global studies by project managing a clinical team at a country level.


    Working throughout the lifecycle of the trial, from start-up through to database lock and closure activities, key responsibilities will include:


    • To manage the local execution of study activities, leading the local trial team of Clinical Research Associates (CRA) and Clinical Trial Assistant; providing them with the necessary tools and training to collectively succeed as a team
    • To serve as the primary point of contact at a country level and report study progress to key stakeholders
    • To lead study start-up process
    • To communicate study status and escalation of relevant deviations and issues concerning e.g. timelines, recruitment, protocol compliance, etc.
    • To develop and implement the use of local study tools (eg recruitment plans, risk management plans)
    • To maintain and update trial management systems
    • To plan and participate in investigator meetings
    • To review visit reports for completeness and adherence to the protocol and to identify site issues and trends
    • To collaborate with other study team members as well as investigators and other site staff to build strong working relationships
    • To perform some visits for key studies (initiation and accompanied visits)



    You are:


    An innovator, motivator and delivery-focused.


    Here at PRA we want our employees to succeed and ensure that they are set up for this success through constant training, development and support. To enable success in this position you will have:


    • A proven track record within study management of clinical trials
    • An ability to combine creativity, leadership and experience to empower a team to succeed
    • Prior experience of on-site monitoring and site management
    • Confidence in your decision-making abilities
    • A current knowledge of processes, legislation and demands in clinical studies
    • A BA or BS degree in a health or science related discipline
    • Fluency in English and local language



    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:


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