Research Coordinator I Ms Clinical Trials Research

2 weeks ago

Toronto, Canada St. Michael's Hospital Full time

The new BARLO MS Centre is a state-of-the-art facility designed to offer coordinated care and research for patients living with MS. It is the largest multiple sclerosis centre in Canada and is home to internationally renowned MS clinicians and researchers.

The MS Clinical Trials team is currently looking for a **Research Coordinator I**. This position performs a variety of research activities which may include assisting in study administration, adhering to research protocol and working with other research team members to carry out various aspects of conducting a clinical trial.

**Duties & Responsibilities**:

- General office duties e.g. filing, faxing, mailings, courier services, photocopying, etc.
- Ordering supplies and maintaining inventory
- Collection, transcription and entry of study related data
- Processing and shipping of laboratory samples to a centralized laboratory (training provided).
- Maintaining study logs (ie: screening, consent, freezer/refrigerator temperature)
- Assist with Research Ethics Board (REB) submissions
- Interacting with various departments such as pharmacy, laboratories, medical records, etc.
- Represent St. Michael’s Hospital at study initiation meetings
- Design of all source documents, patient education materials, etc.
- Coordinating ongoing laboratory, pharmacy, etc. activities pertaining to study
- Assisting Investigators in the interpretation and implementation of study protocols
- Assisting Investigators in the initiation of new research
- Interacting with sponsoring agencies regarding requests for clarifications of data and/or assisting monitors during site visits
- Obtain informed consent for research
- Collecting data via phone calls, interviews
- Screening data for study inclusion according to protocol

**Qualifications**:

- Minimum of Bachelor’s degree in health science field, however Master’s degree would be an asset or demonstrable equivalent combination of specialized education and experience
- At least 2 years clinical trial research experience would be an asset
- 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 verbal and written communication skills
- Excellent computer skills including Word Perfect, Word, Excel, PowerPoint, Internet, database and statistical software

**_

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