PRAHS

  • Medical Advisor Researcher - Laval, Canada (Office Based)

    Job Locations - | Canada-QC
    Posted Date 1 week ago(5/16/2018 9:41 AM)
    ID
    2018-44611
  • 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.

    Responsibilities

    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 leader that isn’t afraid to delegate, but also isn’t afraid to get your hands dirty. You look for new and innovative ways to problem solve. You are the ultimate planner and coordinator and are an excellent communicator. You have a serious passion for clinical development and drug safety. You never settle for what is, but are always pushing clinical development forward to what it could be. You motivate others to do the same. 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.

     

    What will you be doing?

    The Clinical Scientist role is key for medical supervision and medical management of clinical trials in the US. As a Clinical Scientist, you will have a wide range of responsibilities. We’re including a few of the big ones. 

    • Provide support for all Medical Advisors 
    • Assist the Medical Advisors with developing training material and facilitating trainings with CRAs and the study sites 
    • Have regular discussions with Physicians, KOLs, Investigators, and Centers of Excellence 
    • You will be heavily involved in the feasibility process (track the entire process of how many sites have been reached out to, how many sites have responded, what is a good site in the end, etc.)
    • Work directly with the project team to explain the importance of critical scientific data and its intended use

    Qualifications

    What do you need?

    • PhD in biological science or related field, PharmD or MD required 
    • PhD preferred 
    • 5 years of previous CRO/Pharma experience preferred 
    • Exposure to the clinical research environment as a CTL, medical science liaison (MSL), study coordinator, research pharmacist or administrator
    • Must possess a strong clinical background
    • Experience in and knowledgeable about clinical development processes
    • Knowledge of FDA regulations, GCP, ICH
    • Excellent communicator with ability to educate and influence decisions through clear written and verbal communications
    • Proven ability to maintain broad operations and business perspectives
    • Critical strategic thinker, capable of thinking “outside of the box”; innovator and builder
    • Energetic individual, eager to manage multiple activities and priorities
    • Strong organizational skills and detail oriented
    • Proven ability to work independently and in a team environment
    • Self-motivator
    • Dedication to quality in all work tasks and deliverables
    • Experience with relevant computer software (MS Project, Word, Excel, PowerPoint)
    • Read, write and speak fluent French and English; fluent in host country language required

    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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