Job Category: Research InstituteLocationsShowing 1 locationLocationDescriptionPOSITION TYPE:Casual, up to 37.5 hours per weekSALARY SCALE:$34.36 to $39.18 per hourCLOSING 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 PlanWellness program and on-site gymsEmployee and Family Assistance Programincluding Mental health supportProfessional development and learning opportunitiesSummary of the roleThe 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 responsibilitiesImplementation and oversight of clinical research trials from feasibility to closeoutReview new study materials to understand nursing responsibilities and help put these into practice at the clinical trial siteReview, explain and document the patient consenting process related to the studyObtain blood specimensPerform health assessments such as vital signsMix and reconstitute IV medications per research protocolsAdminister intravenous investigational product and monitor for adverse eventsSchedule trial-related procedures such as MRI and PET ScansLiaise with pharmaceutical sponsors, investigators, service providers and the clinical research staffExpected to identify and elevate findings requiring physician reviewReport and follow-up on local adverse events,



serious adverse events and events of special interest in timely mannerAssist in maintaining appropriate on-site storage conditions for investigational productsTrack investigational products and ancillary supplies, including monitoring inventory levels and expiry datesComplete trial-specific source documents as required by protocolParticipate in study, teleconferences and webinars as requiredAssist in drafting informed consents, source documents, ethics applications, funding applications and working templates as requiredAdditional duties may be assigned as appropriateQualificationsRegistered Nurse with a minimum of three (3) years’ experienceCurrent certificate of registration from the College of Nurses of Ontario in good standingCurrent Membership in Registered Nurses' Association of Ontario (RNAO)Current experience in performing venipuncture, phlebotomy, obtaining blood samples, mixing/reconstituting intravenous medications, and administering intravenous medicationsDemonstrated knowledge and ability to utilize the nursing process in planning, implementing and evaluating patient careEvidence of good physical assessment, psychosocial assessment and patient/family teaching skillExcellent organizational and time management skills requiredStrong analytical and problem-solving skillsAbility to work well within a dynamic interdisciplinary teamExcellent interpersonal, verbal and written communication skills requiredAbility to set priorities and work independently with accuracy in a dynamic environmentProficiency with MS Office software - Word and ExcelExperience working with patients with dementia, mild cognitive impairment, and Alzheimer’s diseaseCompletion of ICH/GCP, TCPS2 trainingExperience in clinical cognitive testing, neuropsychological testing, and conducting Electrocardiograms (ECGs)Knowledge of IATA shipping regulations and basic laboratory proceduresClinical research (CCRP)



obtained or plans to work towardsFluent in French and English, an assetThis position will require contact with clinical trial participants who may have a medical illness, cognitive impairment and require special attention. The successful candidate must exhibit empathy and be alert to participant, family member and caregiver needs.Bruyère Health and its Research Institute are fully affiliated with the University of Ottawa, and have other regional academic, government, NGO, and industry partners engaged in team-oriented research and innovation initiatives. Our research priorities include Aging and Long-Term Care, Palliative Care, Rehabilitation and Recovery, and Social Accountability (encompassing Primary Care and Health Equity).Additional Information*Please note that applications received after the closing date will not be considered.This posting is intended to fill an existing vacancy.Bruyère Health uses artificial intelligence to screen and assess answers provided by applicants. All applications received are subsequently reviewed by a member of our team. The information received, including that which is reviewed and analyzed by artificial intelligence, is used and stored in a secure environment and in accordance with Bruyère Health’s privacy policy PHIL 04 - Privacy and Confidentiality of Personal Information.Bruyère Health promotes the principles of diversity and inclusion and adheres to the Employment Equity Act and Accessibility for Ontarians with Disabilities Act. Bruyère Health is committed to developing inclusive, barrier‑free selection processes and work environments. If contacted regarding this competition, please advise the departmental official of the accommodation measures which may be required to enable you to be assessed in a fair and equitable manner.All Bruyère Health employees are required to provide proof of full vaccination for all identified communicable diseases as per our Communicable Diseases: Health Surveillance and Management policy.An acknowledgement of receipt will be sent following the submission of your application. We thank all applicants for their interest, however, only those selected for further consideration will be contacted.#J-18808-Ljbffr

📌 Research Project Coordination Role At Bruyère (Varennes)
🏢 Bruyère Health
📍 Varennes