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Sorry, the application deadline for this position was 8/2/2020

Reference Number: 000001322
Posted Date: 5/26/2020
Closing Date: 8/2/2020

Department: LTRI
Position: Clinical Research Coordinator

POSITION TITLE  Clinical Research Coordinator
EMPLOYMENT TYPE  Temporary Full Time
HOURS OF WORK  37.5 hours per week
REPORTS TO  Principal Investigator


The Department of Psychiatry at Mount Sinai hospital welcomes applications for a Clinical Research Coordinator to work on the busy, dynamic, and growing Perinatal Mental Health Program. The Clinical Research Coordinator will play an integral role in the Scaling Up Maternal Mental healthcare by Increasing access to Treatment (SUMMIT) study, funded by the Patient Centered Outcome Research Institute (PCORI). The SUMMIT trial aims to explore the scalability of one evidence-based treatment—behavioural activation (BA)—for perinatal depression and anxiety. In this role the successful candidate will be responsible for overseeing some of the clinically-oriented research activities of the trial.

Responsibilities of the Clinical Research Coordinator:

  • Scheduling and overseeing key implementation data as related to the intervention delivery 
  • Inventory of clinical research materials and documents
  • File maintenance and safe storage
  • Communication with SUMMIT Treatment Providers Monitor and maintain deadlines and schedules
  • Assist in the preparation of research reports and peer-review process
  • Provide clinical oversight and supervision to clinical research personnel, including ensuring fidelity to treatment, appropriate study documentation and ensuring correct implementation of trial data in accordance of approved ethical procedures.   
  • Participate in team meetings and staff trainings
  • Prepare written correspondence, reports and presentations using Microsoft Word, PowerPoint, Excel and Outlook.


  • Successful completion of a Master’s degree in a clinically-relevant background, ie. Counselling or Clinical Psychology, social work, nursing, etc.
  • Experience interacting with study participants in clinical or mental health settings
  • Strong interpersonal skills with demonstrated verbal and written skills
  • Self-directed with an ability to make decisions and to exercise good judgement
  • Superior organizational and time management skills with a flexibility to adjust to priorities
  • Demonstrated professionalism and ability to work with a variety of individuals in a co-operative manner both independently and as part of a team
  • Ability to work accurately and effectively in a fast-paced environment

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.

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 August 2, 2020. 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


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