PRAHS

  • Lead CRA - Home Based in US (Pre-Recruit)

    Job Locations - | US-Remote
    Posted Date 2 weeks ago(7/11/2018 11:54 AM)
    ID
    2018-47816
  • Overview

    Do you want to watch clinical development change, or do you want to be the one to shape it?

     

    Because we’re hoping you’re here for the latter.

     

    Who are we?

    We Are PRA.

     

    We are 15,000+ employees strong, operating in more than 85 countries. We are committed to saving lives and we are constantly striving to be the best at what we do. Our impact is real and we see it every single day. We are getting live saving drugs into the hands those who need them most.

     

    Who are you?

    You are a forward thinker. You are an innovator that refuses to settle. You want to push the boundaries and change not just what it means to be a Lead Clinical Research Associate, you want to change the future.  You want to learn from the best, grow your knowledge and your skill set, and you want to build your career here. You want to use the latest technology and tools in the industry to push the momentum of an already growing company forward. You want to find a balance that still lets you be, well, you. Most of all, you want to do it in a place where you’re more than an employee number. A place you love working.

     

    Still here? Good. Because if this is you, we’d really like to meet you.

    Responsibilities

    What will you be doing?

     

    As a Lead Clinical Research Associate, you will be accountable for achieving successful delivery of clinical activities at the project level by meeting internal and external contractually agreed client and regulatory requirements according to time, quality/scope and budget constraints. The CTM leads and directs cross functional teams (Clinical Operations, Regulatory Affairs) and understands/manages client expectations. The CTM proactively identifies, resolves/mitigates and escalates risks and/or issues. Depending on the business unit the descripted accountabilities may or may not apply.

     

    • Applies knowledge of PRA’s policies and procedures
    • Manages international clinical teams and multiple trial deliverables
    • Demonstrates excellent written and oral communication with internal/external teams and with the customer
    • Reads, writes and speak fluent English; and is fluent in host country language
    • Demonstrates excellent knowledge of ICH/GCP
    • Utilizes clinical knowledge to develop and implement task and trial specific training
    • Accurately projects work and resourcing requirements
    • Interactions with multi-functional teams and with the sponsor
    • Contributes to the preparation and presentation of bid defenses
    • Understands associated functions as they relates to Clinical/Trial Management
    • Demonstrates working knowledge of Microsoft Office applications, Clinical Trial Management Systems, and Electronic Data Capture platforms

     

    Qualifications

    What do you need to have?

     

    Education: 

    • Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience required.

    Skills: 

    • 3+ years of clinical research experience required
    • Read, write and speak fluent English; fluent in host country language required.
    • 2+ years monitoring experience preferred

     

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

     

    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.

     

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