|  Home  |  Lunenfeld-Tanenbaum  |  Hospital  |  Foundation  |

  Lunenfeld-Tanenbaum CV Bank Opportunities  
CV Bank — Human Resources
Sorry, the application deadline for this position was 1/28/2020

Reference Number: 000001275
Posted Date: 12/3/2019
Closing Date: 1/28/2020

Department: LTRI (Rheumatology)
Position: Research Coordinator I

POSITION TITLE Research Coordinator I
DEPARTMENT LTRI (Rheumatology)
EMPLOYMENT TYPE Temporary Full Time
HOURS OF WORK 37.5 hours per week
REPORTS TO Principal Investigator

This is a temporary full-time opportunity for up to 12 months with the possibility of extension.


We are seeking a strong and highly motivated Research Coordinator I to facilitate the clinical research activities within a rheumatology setting.  Specific tasks will include: clinical trial coordination, drafting clinical research documents (REB applications/protocols), data abstraction and database management, manuscript preparation, creating informed consent forms and preparing education materials.


  • Recruit and obtain informed consent from potential research subjects, coordinate clinical trials through both MSH and UHN
  • Conduct data abstraction/collection from patient charts, including pulmonary function tests, ECG, echocardiogram, laboratory tests and CT scans
  • Perform accurate and timely data entry into clinical research database
  • Interact with study participants in the clinic for research consent and for education purposes
  • Complete REB, contract submissions and Health Canada submissions
  • Prepare for monitor, Health Canada and/or FDA audits
  • Collaborate in the preparation of manuscripts and other research submissions, including drafting methods sections, managing references and coordinating submissions
  • Manage research finances


  • Minimum BSc in health sciences discipline
  • Post Graduate Certificate in Clinical Research or Certified Clinical Research Professional (CCRP) required
  • Minimum of 3 years of experience in a clinical research setting
  • Experience coordinating clinical trials at a hospital level, including recruitment, conducting prospective participant interviews, extracting source data and study coordination
  • Must have excellent interpersonal skills and be willing to interact with patient population
  • Strong ability to work in a multi-disciplinary team in a cooperative manner
  • Must be able to set priorities and work independently with minimal direction
  • Must possess excellent verbal, written and interpersonal communication skills
  • Proficiency with MS Office software required


Posting open until January 28, 2020. We thank all candidates for applying. Only those selected for an interview will be contacted.

Hours: 37.5 hours of work

Contact Name: Online
Contact Email: Online
Contact Phone: Online
Contact Fax: Online


Returning Applicants?
Just a reminder — this Website requires that you sign-on to fill out application forms and to upload files. The sign-on link is located in the top-right corner of this page.
New Applicants?
If you are new to this Website and do not have an ID, the sign-on script will allow you to create one — just click the sign-on link located in the top-right corner of this page and follow the on-screen instructions; or click the link here directly to create a User ID.