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Clinical Research Coordinator Ii
3 months ago
Start date:
As soon as possible.
Term:
One-year contract.
Responsibilities:
- Coordinate and implement investigator initiated, low to moderate risk clinical, research protocols.
- Monitors the ongoing clinical status of patients, assessing for adverse events while they are receiving study interventions
- Prepare and maintain patient research files, complete case report forms, data entry, schedule appointments.
- Performs accurate data collection with extraction from health records.
- Assist with various aspects of clinical research projects as required by Manager.
Requirements:
- Minimum of 3 years of experience in a clinical research setting, including trial recruitment and operations.
- BSc in a healthrelated field or equivalent work experience.
- Evidence of training certification in Tri-Council Policy Statement2 (TCPS2) and the International Council on Harmonisation
- Good Clinical Practice Guidelines (ICH-GCP).
- Ability to work onsite at the Heart Institute.
Preferred qualifications:
- Previous experience in research related to nicotine, tobacco, and/or ecigarettes is an asset.
- Excellent computer skills; demonstrated ability to modify/edit documents using track changes. Required computer skills in Word, Excel, PowerPoint.
- High personal motivation, selfmanagement, and detailorientation; ability to take responsibility in meeting deadlines and making progress without direct supervision.
- Strong spoken and written communications skills.
To apply:
The University of Ottawa Heart Institute is committed to ensuring barrier-free selection processes and work environments. Accommodations will be provided in all parts of the hiring process relating to any specialty requirements.
Please notify us of any accommodations that you require - any information you provide will be handled respectfully and in complete confidence.
