Job description
ResponsibilitiesCoordinate and implement investigator initiated, low to moderate risk clinical, research protocols.Provide support to clinical research nurse coordinator in the implementation of multi centre or larger complex clinical research projects.Identify, screen, consent and follow up of eligible research subjects as appropriate to skill level.Monitors progress and ensures comprehension of the study protocol by the candidate and participating personnel.Monitors the ongoing clinical status of patients, assessing for adverse events while they are receiving study interventions which may involve investigational therapies.Prepare and maintain patient research files, complete case report forms, data entry, schedule appointments.Prepare applications, renewals or amendments for REB Committee review; assist with and maintain up to date REB filing for all projects.Performs accurate data collection with extraction from health records.Assist with various aspects of clinical research projects as required by Manager.
Responsibilities & skills
Motivation to engage in and manage a wide range of intellectual and physical work, ranging from basic data entry to active screening and recruitment of study subjects as appropriate.
Education
Excellent computer skills; demonstrated ability to modify/edit documents using track changes. Required computer skills in Word, Excel, PowerPoint.Previous experience with EPIC EMR system.High personal motivation, self-management, and detail-orientation; ability to take responsibility in meeting deadlines and making progress without direct supervision.
Experience
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University of Ottawa
The University of Ottawa is the largest bilingual university in the world, where it is possible for students to study in English, in French, or in both languages. Located in the capital of Canada, a G8 nation, we have ready access to the great institutions of our country.
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