PRAHS

  • Senior Clinical Trial Liaison_ Shanghai

    Job Locations (All) | China
    Posted Date 2 months ago(1/6/2019 10:22 PM)
    ID
    2019-51323
  • Overview

    At PRA, we don’t make our 15000+ people great. It’s the other way around. As we have grown to a top-5 CRO, we have maintained the feel of a small company, dedicated to collaboration and passion for what we do.

     

    We always have a desire to keep seeking new and better ways to operate. We don’t settle for the same old ways. Our passion for improving patient lives worldwide permeates all that we do. Put simply, we care.

    Responsibilities

    We are currently looking for a Senior Medical Trial Liason to be based in Shanghai.

     

    The Clinical Trial Liaison will foster relationships with clinical investigators and other professionals at the site level to optimize patient recruitment for clinical trials that PRA is the lead CRO. The CTL has a thorough understanding of the investigational agents being used in the study, the trial’s eligibility criteria, and all study procedures. In addition, the CTL will work with sites to optimize performance and communicate with PRA employees and strategize with the sites to make sure patient recruitment, data quality and protocol requirements are being followed. Repeated interactions will be needed over the course of the trial to ensure that trial remains “top of mind” with investigators and staff. The CTL will function as part of the study team and will interact frequently with sponsor companies and their field personnel. Furthermore, the CTL will serve as liaison with key investigators to help ensure that they receive prompt assistance with any queries and that any concerns they have are promptly transmitted to the trial’s sponsor.  The CTL's responsibilities will include:

    • Understand the scientific basis of assigned clinical trials
    • Create educational materials to effectively communicate the science behind the clinical trial
    • Be able to communicate the scientific basis of the trials to other team members, investigators and site staff
    • Identify effective prescreening strategies for each trial and recommend improvements
    • Provide detailed reports of interactions with investigators and site staff
    • Serve as a therapeutic expert for internal PRA staff
    • Serve as the team lead for studies employing multiple CTLs
    • Provide education and mentoring to other CTLs
    • Participate in business development activities as assigned

    Qualifications

    You are:

    An expert in your field with an affinity to lead and inspire.

    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 the following:

    • PhD or MD in biological science required
    • Read, write and speak fluent English; fluent in host country language required
    • Clinical Trial Liaison or Medical Science Liaison experience preferred
    • Exposure to the clinical research environment as a CTL, medical science liaison (MSL), study coordinator, or research pharmacist  preferred

    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.

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