PRAHS

  • Sr. Clinical Trial Manager - Global Trial Management, Clinical Technology (Home-Based)

    Job Locations - | US-Remote
    Posted Date 2 weeks ago(8/3/2018 11:40 AM)
    ID
    2018-48418
  • Overview

    As a top five CRO, we have worked on 100+ marketed drugs across several therapeutic areas and conducted the pivotal or supportive trials that led to FDA and/or international regulatory approval of 45+ such drugs.

     

    At PRA Health Sciences, providing innovative solutions for our clients is what we do. From full service clinical development to the pioneering Embedded SolutionsTM model, PRA provides a broad spectrum of solutions that meet the demands of a diverse marketplace.

     

    At PRA, borders do not create boundaries.  PRA’s success is dependent upon our ability to attract and retain a talented team of diverse professionals.  Our growing workforce is comprised of over 15,000 employees, spanning 13 time zones across six continents and who speak more than 30 languages – yet operate in unison as one worldwide PRA community.

     

     

    Responsibilities

    The Senior Clinical Trial Manager is responsible for the global coordination of clinical trial management activities for internally managed and/or outsourced trials. Responsibilities also include management of global vendors involved in site facing activities such as IVRS, Central Lab, ePRO, Imaging, Translation, Printing, Ancillary supplies and Meeting Planners. This position leads the Study Management Team (SMT) and interfaces with stakeholders internal and external to Global Clinical Development Operations (GCDO) functions, such as Study Responsible Physician, Global Data Manager, Trial Supply Manager, CRO staff, vendor staff and Study Sites (if applicable). He/she works closely with the GCDO Trial Leader (GTL) and is member of the Trial Team, led by the GTL. At the Senior level, a CTM is given assignments that are more complex and/or have a greater potential impact on business results. May act as the lead over a team of CTMs across a project/program, on insourced and outsourced studies. Able to lead taskforces and provide innovative input.

    Qualifications

    REQUIRED EXPERIENCE:

    • Minimum 5 years experience in clinical research, including a minimum 2 years  project management experience or an equivalent combination of education and experience sufficient to successfully perform the key responsibilities of the job.
    • Reads, writes and speaks fluent English; fluent in language of host country.
    • Strong understanding and expeirence working with patient centered clinical technology
    • Experience managing and/or working with global clinical trials
    • A graduate degree or undergraduate degree.

    PREFERRED EXPERIENCE:

     

    • Experience with patient centered clinical trial technology highly preferred
    • Experience leading/driving patient engagement
    • An undergraduate degree with 7 years of experience in clinical research and at least 3 years as a clinical project manager. 
    • Or a Graduate degree with 5 years of experience in clinical research and at least 2 year as a functional team lead role or single service project management.


    To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status.


    PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.

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