Study Designer - Laval, Canada - Altasciences

    Altasciences
    Altasciences Laval, Canada

    Found in: Talent CA C2 - 1 week ago

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    Description

    Study Designer

    Laval, QC, Canada ● Montreal, QC, Canada Req #4523 Wednesday, April 10, 2024

    Your New Company
    At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences. We are better together and together We Are Altasciences.

    Your Role:

    The Study Designer is responsible for the design/creation and maintenance of source used to capture data during clinical trials either on a paper format or within an Electronic Data Capture (EDC) system. The Study Designer will conduct tasks performed within compliance of study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs).

    What you ' ll do here:

  • Ensure the confidentiality of clinical trial volunteers and sponsors is respected.
  • Maintain and advocate a high level of quality and customer service within the department.
  • Understand protocol driven timed study events and acceptable collection windows (protocol and/or SOP driven) for the timed events.
  • Review clinical trial protocols/manuals and SOPs to assess criteria that needs to be captured during clinical trial execution.
  • Maintain a continuous line of communication with clinical operations teams and data management teams on the progression of clinical study designs.
  • Perform internal reviews of clinical study designs.
  • Maintain a library of general template designs.
  • Provide clinical study designs to clinical operations teams for review/approval in a time efficient manner.
  • Proactivelycommunicateissues and/or problem resolutions to departmental supervisors and managers.
  • Complete and/or maintain training as required per jobs needs.
  • Attend and/or participate in meetings (i.e. protocol, study design).
  • Performgeneral administrative tasks when required.
  • What you need to succeed.

  • Completed DEC in one of the following fields: computer science or sciences;
  • Excellent communication skills in French and English;
  • Knowledge and/or experience with protocols an asset;
  • Knowledge of Clin Spark or EDC an asset;
  • Detail oriented;
  • Well organized;
  • Customer service focused;
  • Able to work in fast-paced environment.
  • What We Offer

  • Regular full-time position;
  • 37.5 hours/week
  • Remote position.
  • Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives bothat and outside of work.

    Altasciences' Benefits Package Includes:


    • Health/Dental/Vision Insurance Plans


    • RRSP with Employer Match


    • Paid Vacation and Holidays


    • Paid Sick and Bereavement Leave


    Altasciences' Incentive Programs Include:


    • Training & Development Programs


    • Employee Referral Bonus Program

    MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH