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Research Coordinator I

2 weeks ago

Toronto, Canada St. Michael's Hospital Full time

The position allows for flexibility in working hours and the possibility of extension after 1 year.

**Duties & Responsibilities**:

- Interpretation and implementation of research protocols
- Performing telephone screening for study inclusion according to study protocols
- Interacting with hospital departments such as the CF Clinic, Pulmonary Function Lab, Research Ethics Board, Contracts, Finance etc.
- Obtaining informed consent from study participants (both over the phone and in person)
- Administering on-line survey instruments
- Collecting data during study visits with participants
- Monitoring and reporting adverse events and serious adverse events
- Maintenance, transcription and entry of study related data
- Performing general office duties e.g. filing, faxing, mailings, courier services, photocopying, etc.
- Assisting the Principal Investigator in the initiation of new research (including preparing submissions to the research ethics board) and setting project goals

**Qualifications**:

- Minimum of Bachelor’s degree in health science field, however Masters preferred
- Minimum of 2 year clinical research assistant experience
- Excellent communication (verbal/written) and interpersonal skills are necessary
- Excellent attention to detail and proven ability to learn new skills
- Superior organizational skills to manage multiple projects in a timely manner and flexibility to adapt to changing workload
- Professionalism and self-motivation
- Good personal and program time/detail management skills
- Able to work independently and as part of a team
- Excellent computer skills (MS Office Suite)

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