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Clinical Research Coordinator(100220)

Sunnybrook Health Sciences Centre

This is a Contract position in Toronto, ON posted November 1, 2020.

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Clinical Research Coordinator (100220) Toronto, ON, CA Posted: 10/2/2020 9:29:40 AM

Sunnybrook Research Institute (SRI) is seeking a temporary full time Clinical Research Coordinator to collaborate with physicians and multidisciplinary health care team members to carry out a variety of research activities in the field of Transfusion Medicine. While the specific requirements of each project will vary, the position may at different times involve the following activities:

The Research Coordinator assists in the recruitment of study participants (e.g. identifies and screens potential subjects, obtains informed consent, conducts pre-testing and administers questionnaires or other data collection tools); assists in planning, implementation and coordination of all aspects of data collection and source documentation, as per ICH/GCP guidelines; conducts telephone and/or clinical recruitment interviews to collect data using established criteria; coordinates patient visits schedule as per study protocol; assists in study visits (e.g. assessment, adverse events, monitoring safety, medication, questionnaires, sample collection, processing and shipment of samples according to clinical protocol); plans, designs and organizes scoring procedures and computer databases for ongoing and new research studies; may perform computer statistical analyses and generate response curves, status reports; coordinating research activities and ethics submissions in collaborating hospitals; and other administrative duties including those associated with the grant.

QUALIFICATIONS

  • Bachelor’s degree in health related field or equivalent
  • Five (5) years clinical research experience
  • Knowledge of research regulations and guidelines, such as ICH/GCP guidelines, Tri-Council Policy, Declaration of Helsinki and FDA CFR and Health Canada TPD
  • Experience and expertise in recruiting patients required to clinical trial
  • Proven ability to work independently, and as part of a clinical research team
  • Experience using statistical analysis and data management software applications required
  • Excellent communications/interpersonal skills
  • Excellent organizational skills with strong attention to detail

Qualified candidates are invited to submit a CV and cover letter to Chantal Armali at Chantal.armali@sunnybrook.ca. Please include “Research Coordinator” in the subject line.

We thank you in advance for your interest. Only those candidates selected for an interview will be contacted.

In accordance with Canadian Employment and Immigration guidelines, applicants must be eligible to work in Canada. Sunnybrook Research Institute is committed to providing accessible employment practices that are in compliance with the Accessibility for Ontarians with Disabilities Act (AODA). If you require accommodation for disability during any stage of the recruitment process, please indicate this in your cover letter.

Sunnybrook Research Institute is strongly committed to inclusion and diversity within its community and welcomes all applicants including but not limited to: visible minorities, all religions and ethnicities, persons with disabilities, LGBTQ2+ persons, and all others who may contribute to the further diversification of ideas.

Sunnybrook Research Institute is committed to providing accessible employment practices that are in compliance with the Accessibility for Ontarians with Disabilities Act (AODA). If you require accommodation for disability during any stage of the recruitment process, please indicate this in your cover letter.

Sunnybrook Research Institute is strongly committed to inclusion and diversity within its community and welcomes all applicants including but not limited to: visible minorities, all religions and ethnicities, persons with disabilities, LGBTQ persons, and all others who may contribute to the further diversification of ideas.

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