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    Research Coordinator 2 - Toronto, Canada - Baycrest

    Baycrest
    Baycrest Toronto, Canada

    2 days ago

    Default job background
    Temporary
    Description
    Responsibilities include but are not limited to:Responsibilities include but are not limited to:
  • Serve as primary contact for multiple studies/sites
  • Recruit and screen patients for eligibility for current studies based on established protocols
  • Conducts and documents informed consent process
  • Monitor subject's progress and report adverse events
  • Generate study specific case report forms (CRFs)
  • Record study data into CRFs, query resolution and responding to data queries
  • Manage Research Data Bases
  • Maintain Clinical Trial Management System
  • Prepare for and conduct study monitor visits and audits
  • Serves as a liaison to physicians, investigators, patients and other staff members regarding the research process and individual protocols
  • Submit and Review Institutional Review Board documents
  • Strategizes and helps troubleshoot to correct problems
  • Escalates issues as needed to supervisor

    • Qualifications include but are not limited to:

  • Clinical Research Experience (2+ years)
  • Current GCP and familiarity with Health Canada, FDA, ICH GCP regulations
  • Current GCP, Health Canada Part C Division 5, IATA certifications
  • Bachelor's Degree or 4 years relevant professional experience in lieu of degree
  • Experience with Microsoft Office (Word, Excel, Power point, etc.)
  • Have a true passion to work in Clinical Trials
  • Phlebotomy certification
  • Comfortable in the lab setting (Centrifuge/pipetting)

    • Required Skills:

  • Excellent organization and attention to detail
  • Quick and eager learner
  • Ability to work independently
  • Strong critical thinking
  • Excellent oral and written communication
  • 2+ years of experience in related field
  • Working knowledge of research methodology/medical terminology
  • Meticulous work ethic and attention to detail, with excellent time-management and organizational skills.
  • Ability to manage competing demands of short and long-term projects led by numerous individuals, directing multiple varied assignments, independently coordinating and prioritizing relevant projects, tasks and responsibilities.
  • Highly motivated and adaptable with an ability to take initiative and work well independently and as part of a multidisciplinary team.
  • Ability to produce high quality work while meeting deadlines in accordance to CTU standards.
  • Ability to maintain confidentiality.
  • Certification as a Clinical Research Professional

    • Additional Benefits:

  • 4% Vacation
  • Opportunity to enroll in the Healthcare of Ontario Pension Plan (HOOPP)
  • Access to 24/7 Employee Assistance Program
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