• Clinical Research Manager (CRM)

    Job Locations - | Turkey
    Posted Date 2 months ago(6/11/2018 9:38 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 lifesaving 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.


    As a Clinical Research Manager you will be dedicated to one of our global pharmaceutical clients; a company that is advancing the development of new medicines, biologic therapies and vaccines for many of the world’s most challenging diseases including cancer, cardio-metabolic diseases, Alzheimer’s and infectious diseases. Be ready to work in a solid partnership and an environment driven by innovation and continuous improvement.


    Typical responsibilities:

    • Act as a country point of contact for assigned protocols and proactively drive/track execution and performance of deliverables/timelines/results to meet country commitments;
    • Forecast country resource needs and serve local business needs;
    • Responsible for quality and compliance of assigned protocols in the country and oversee CRA’s and CTC’s training compliance;
    • Perform quality control visits, review Monitoring Visit Reports and escalate performance issues and training needs to functional vendor and internal management as needed;
    • Responsible for collaboration and relationship management with investigators for insourced studies, with functional outsourcing vendors and other external partners;
    • Oversee country and site validations, site selection and recruitment in assigned protocols;
    • Responsible for clinical trial education to sites.

    As a Clinical Research Manager, you will have the opportunity to experience the full lifecycle of a project and genuinely contribute to drug development and improving patients’ lives.


    You are:


    Confident, responsible and have a fantastic communication skills.


    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:


    • Strong interpersonal skills and organizational skills
    • Strong understanding of clinical trial planning (site) management and metrics
    • Strong leadership skills
    • A quality-focused mindset
    • 5 + years of experience in Clinical Research
    • Bachelor’s degree or Master’s degree or equivalent / PhD or MD
    • Fluency in written and spoken English

     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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