|  Home  |  Lunenfeld-Tanenbaum  |  Hospital  |  Foundation  |

  Lunenfeld-Tanenbaum CV Bank Opportunities  
CV Bank — Human Resources
Sorry, the application deadline for this position was 5/7/2021

Reference Number: 000001457
Posted Date: 4/23/2021
Closing Date: 5/7/2021

Department: LTRI - Zane Cohen Centre
Position: Clinical Research Assistant III

POSITION TITLE  Clinical Research Assistant III
DEPARTMENT  LTRI - Zane Cohen Centre
EMPLOYMENT TYPE  Temporary Full Time
HOURS OF WORK  37.5 hours per week
REPORTS TO  Principal Investigator and Project Manager

The Lunenfeld-Tanenbaum Research Institute of Mount Sinai Hospital, a University of Toronto affiliated research centre, is one of the world's leading centres in biomedical research.  With ground-breaking discoveries in research areas such as diabetes, genetic disorders, cancer and women’s and infants’ health, the Institute is committed to excellence in health research and the training of young investigators.  Strong partnerships with the clinical programs of Mount Sinai Hospital ensure that scientific knowledge is used to promote human health.  Your significant contributions will assist in maintaining our momentum in advancing our research.


The goals of Dr. Silverberg’s research program are to identify susceptibility genes and biomarkers for IBD and to explain the contribution of these markers to its etiology and clinical course. More recently, we are also investigating the host microbiome in association with complex disease.

For more information about our research, please visit our websites at: or


A Temporary, full-time position (Mon.-Fri., hours must be flexible) is available in Dr. Silverberg’s clinical translational group at the Lunenfeld-Tanenbaum Research Institute of Mount Sinai Hospital.

As a member of the research team, the Clinical Research Assistant collaborates with Investigators and the health care team in the coordination of clinical research. Studies may include pharma-sponsored, cooperative group sponsored, and investigator-initiated studies. Under the direction of principal investigators and project managers, the Clinical Research Assistant will implement clinical research studies, which typically include subject identification and recruitment, obtaining informed consent, clinical assessment for study eligibility, study education, sample collection and follow-up with participants.

In this position, the successful candidate will contribute through the effective recruitment of subjects to our various studies. A successful candidate is expected to acquire knowledge regarding IBD, IBD related surgeries, medications and terminology quickly as well as to work well with other members of the team and be an excellent communicator. The successful candidate must be flexible with work hours (some days will start very early and/or end very late). The Clinical Research Assistant may participate in meetings, and perform other related duties as assigned. This person will report to the Project Manager and the PI.


  • Bachelor’s degree in a health or science related discipline with a minimum of two years clinical research experience
  • Master’s degree (MSc) in a health or science related discipline preferred
  • High degree of computer literacy and extensive experience with Microsoft Office (Word, and Excel)
  • Existing phlebotomy certification
  • Ability to manage multiple studies at a time and modify job responsibilities as required
  • Knowledge of medical terminology
  • Ability to work independently, effectively and efficiently as well as good interpersonal skills with the ability to work as a team member
  • Familiarity in working with confidential information; maintaining professionalism, diplomacy and tact under high pressure situations
  • Must be able to work flexible hours and work on your feet for hours at a time
  • Autonomous critical thinking ability
  • Excellent organizational and time management skills required
  • Strong analytical and problem-solving skills
  • Self-motivated, detail-oriented
  • Excellent interpersonal, verbal, and written communication skills required

In accordance with Institute’s policy and legislated health and safety requirements, employment is conditional upon the verification of credentials, completion of a health review, and demonstrating proof of immunity and vaccination status of vaccine-preventable diseases. Successful candidates will be required to provide two (2) written reference letters from their former employer(s)/supervisor(s).

We are a fully committed to fairness and equity in employment and our recruitment and selection practices. We encourage applications from Indigenous peoples, people with disabilities, members of sexual minority groups, members of racialized groups, women and any others who may contribute to the further diversification of our Sinai Health community. Accommodation will be provided in all parts of the hiring process as required under our Access for People with Disabilities policy. Applicants need to make their requirements known in advance.

The Lunenfeld-Tanenbaum Research Institute is a scent sensitive environment, and all members of the community are expected to refrain from wearing or using scented products while visiting or working at the Institute. We also support a barrier-free workplace supported by the Institute’s accessibility plan, accommodation and disability management policies and procedures. Should you require accommodation at any point during the recruitment process, including accessible job postings, please contact the Lunenfeld-Tanenbaum Human Resources Department.

Posting open until May 7, 2021. We thank all candidates for applying. Only those selected for an interview will be contacted.

Hours: 37.5 hours per week

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.