Research Coordinator 1

3 weeks ago


Toronto, Canada Baycrest Full time
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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