Research Coordinator Ii Nephrology Research

2 weeks ago


Toronto, Canada St. Michael's Hospital Full time

The Coordinator Class represents staff that performs research activities involving project design, and collecting, summarizing and/or analyzing data. They may assist in study administration. This position requires the ability to adhere to research protocol and work with the study coordinator/Investigator to carry out various aspects of conducting a clinical trial.
- Reports to higher level coordinators, research associate and principal investigator.
- All positions must be flexible to work beyond the job description at times as work demands.
- Exercise flexibility in working hours to adjust for weekend and/or off hour requirements.

**Duties/Responsibilities**:
This position includes all of the duties/responsibilities of the Coordinator I position, as well as:
**Clerical/Support ( 50% of work time)**
- oversee the collection and transcription of study-related data and/or reviewing data previously transcribed by other research staff
- assist investigators in the initiation of new research
- assist investigator in the interpretation and implementation of study protocols
- ongoing communication with representatives at sponsoring agencies/firms
- prepare REB submissions relative to the initiation and conduct of individual studies
- consent form design and revisions
- represent St. Michael’s Hospital at protocol development and study initiation meetings

**Research Activities (40% of work time)**
- conduct interviews with research participants
- standardized questionnaire administration
- collecting data via phone calls, interviews
- administration of the Letter of Information and Consent Form to study participants
- education of participants re: treatment schedule and/or the use of data collection tools
- If qualified and/or applicable, may include specialized clinical duties such as: withdrawal of blood for study-related blood work or study-related pharmacokinetic analysis; nutritional assessment; mobility assessment; initiation of IV’s; physical assessment of patients including assessment of physical systems and assessment of adverse events
- Analysis of data, including use of programming languages (eg. R, Matlab) for this purpose

**Managerial (10% of work time)**
- oversee the ongoing collection, tabulation and analysis of study related data and ongoing review and development of study databases
- encourage a team approach within the group and promoting a cross-functional approach with other divisions within the hospital
- ensure payments are forthcoming during conduct of study
- ensure appropriate regulations are adhered to in the conduct of research
- present research related information including written study reports where necessary

**Qualifications, Knowledge and Skills**:

- Minimum Bachelor of Science (preferably with 5 years related research experience), preferably Masters Degree (with 3 years related research experience), or demonstrable equivalent combination of specialized education and experience
- Experience with programming languages (R, Python and/or Matlab) strongly preferred
- Prior experience with analysis of “big data” (eg. RNA-Seq)
- meticulous and capable of independent decision making with study data

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