Lunenfeld-Tanenbaum Research Institute Clinical Research Coordinator I Part Time in Toronto, ON

Overview

Lunenfeld-Tanenbaum Research Institute

Branch Toronto ON CA

Position:
Clinical Research Coordinator I
Location:
Toronto, ON

The study sites include Sinai Health System, University Health Network, St Michael’s Hospital, and Sunnybrook Health Sciences Centre….

Reference Number: 000000899
Posted Date: 3/29/2017
Closing Date: 4/12/2017

Department: Department of Medicine
Position: Clinical Research Coordinator I

POSITION TITLE
Clinical Research Coordinator I

DEPARTMENT
Department of Medicine

EMPLOYMENT TYPE
Temporary Part Time (24 Months)

HOURS OF WORK
30 hours per week, requires some flexibility

EMPLOYEE GROUP
Non-Union

REPORTS TO
Clinician Scientist

ORGANIZATION OR DEPARTMENT DESCRIPTION:
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.

Research Project Overview

We are conducting a knowledge translation quality improvement study to reduce unnecessary sedative prescriptions among hospitalized patients across 4 academic medical centres (AMCs). The study sites include Sinai Health System, University Health Network, St Michael’s Hospital, and Sunnybrook Health Sciences Centre. The principle and co-investigators are affiliated with the University of Toronto.

JOB RESPONSIBILITIES:
Overseeing the coordination of quality improvement project roll-out across 4 AMCs

Conduct literature reviews, as required

Complete necessary REB applications, documentation Manage data collection by research assistants at each site

Over-see the collection, coding, entry of quantitative and qualitative data

Maintaining accurate research records and database

Experience and Education

Master’s degree or equivalent, preferrably in clinical investigation or health services research.

Previous experience in quality improvement evaluative studies in an academic or clinical setting is required.

A working knowledge of Word, Excel and SPSS or STATA is an asset.

Ability to work independently, effectively and efficiently

Excellent organizational, communication, and time management skills

Outstanding attention to detail and management skills

Experience with clinical healthcare-related quality improvement research

Please apply to: [email protected]