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Research Project Specialist 2 Health RI_Nurse
Job Description & How to Apply Below
Job Category :
Research Institute
Locations
Showing 1 location
Location
Description
POSITION TYPE: Casual, up to 37.5 hours per week
SALARY SCALE: $34.36 to $39.18 per hour
CLOSING DATE: 2026/09/04
* The Bruyère Health Research Institute supports investigators who contribute to a better, more responsive health care system that delivers the best care to patients, residents, and families. We focus on finding the future of care for aging Canadians and vulnerable populations.
What we offer?
Defined Pension Plan
Wellness program and on-site gyms
Employee and Family Assistance Program including Mental health support
Professional development and learning opportunities
Summary of the role
The Clinical Trials Portfolio of Bruyère Health RI is a rapidly expanding group which encompasses clinical trials research in various therapeutic areas with a focus on brain and mind research. We are currently seeking a highly motivated, organized, enthusiastic individual to join our dynamic team. Under the immediate supervision of the Principal Investigator and the Research Manager, the incumbent is responsible for supporting the successful conduct and coordination of studies that could include pharma-sponsored or investigator-initiated trials.
If you are interested in a specialized nursing role in research that is challenging, stimulating and provides autonomy within a strong collaborative team, this could be the role that you are looking for.
Main duties and responsibilities
Implementation and oversight of clinical research trials from feasibility to closeout
Review new study materials to understand nursing responsibilities and help put these into practice at the clinical trial site
Review, explain and document the patient consenting process related to the study
Obtain blood specimens
Perform health assessments such as vital signs
Mix and reconstitute IV medications per research protocols
Administer intravenous investigational product and monitor for adverse events
Schedule trial-related procedures such as MRI and PET Scans
Liaise with pharmaceutical sponsors, investigators, service providers and the clinical research staff
Expected to identify and elevate findings requiring physician review
Report and follow-up on local adverse events, serious adverse events and events of special interest in timely manner
Assist in maintaining appropriate on-site storage conditions for investigational products
Track investigational products and ancillary supplies, including monitoring inventory levels and expiry dates
Complete trial-specific source documents as required by protocol
Participate in study, teleconferences and webinars as required
Assist in drafting informed consents, source documents, ethics applications, funding applications and working templates as required
Additional duties may be assigned as appropriate
Qualifications
Registered Nurse with a minimum of three (3) years’ experience
Current certificate of registration from the College of Nurses of Ontario in good standing
Current Membership in Registered Nurses' Association of Ontario (RNAO)
Current experience in performing venipuncture, phlebotomy, obtaining blood samples, mixing/reconstituting intravenous medications, and administering intravenous medications
Demonstrated knowledge and ability to utilize the nursing process in planning, implementing and evaluating patient care
Evidence of good physical assessment, psychosocial assessment and patient/family teaching skill
Excellent organizational and time management skills required
Strong analytical and problem-solving skills
Ability to work well within a dynamic interdisciplinary team
Excellent interpersonal, verbal and written communication skills required
Ability to set priorities and work independently with accuracy in a dynamic environment
Proficiency with MS Office software - Word and Excel
Experience working with patients with dementia, mild cognitive impairment, and Alzheimer’s disease
Completion of ICH/GCP, TCPS2 training
Experience in clinical cognitive testing, neuropsychological testing, and conducting Electrocardiograms (ECGs)
Knowledge of IATA shipping regulations and basic laboratory procedures
Clinical research (CCRP) obtained or plans to…
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