Clinical Research Coordinator Iii (Phase 1) (Toronto)

Clinical Research Coordinator Iii (Phase 1) (Toronto)

31 Aug
|
University Health Network
|
Toronto

31 Aug

University Health Network

Toronto

Union: Non-UnionNumber of Vacancies: 1New or Replacement Position: ReplacementSite: Princess Margaret Cancer CentreDepartment: CancerClinical Research Unit (CCRU) NursingReports to: Clinical Research Nurse ManagerSalary Range: $84,779 - $105,968 Per YearHours: 37.5 Hours Per WeekShifts: Monday-FridayStatus: Permanent Full-timeClosing Date: June 24, 2026Position SummaryThe Clinical Research Coordinator collaborates with Investigators and health care team to assume responsibility for the overall patient management and coordination of several clinical studies for the Drug Development Program at Princess Margaret Cancer Centre. The research nurse will work primarily in the Phase 1 clinical trials group. Studies include pharma-sponsored, cooperative group sponsored (such as NCIC) as well as Investigator initiated trials.DutiesRecruitment of study participants (e.G. identify and screen potential subjects, obtain informed consent)Coordination of patient visits schedules as per study protocol; execution of all aspects of study visit (e.G. assessment adverse events, monitoring safety, medication, questionnaires, sample collection, including processing and shipment of samples according to clinical protocol, assessments, vital signs, ECG’s, monitoring and administration of treatments as per study protocol).Provides clinical care for patients participating in clinical trials and the implementation and coordination of all aspects of data collection and source documentation, as per UHN policy and ICH/GCP guidelines.QualificationsBachelor’s degree, or recognized equivalent, and current certificate of competence (licensure/registration) from a college legislated under the Regulated Health Professions ActAt minimum 3 to 5 years clinical and/or professional experience is requiredCurrent registration with the College of Nurses of OntarioRecognized certification in clinical research (ACRP or SOCRA) obtained or plans to work towardsRegistered Nurse with a minimum of 3 (three)



years experienceStrong knowledge base in Phase I Clinical TrialsChemotherapy certification (deSouza Institute) is preferredDemonstrated 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 skillTraining in ICH/GCP guidelines is an assetKnowledge of IATA shipping regulations and basic laboratory procedures an assetExcellent organizational and time management skills requiredStrong analytical and problem solving skillsExcellent interpersonal, verbal and written communication skills requiredAbility to set priorities and work independently with accuracy in a agile environmentProficiency with MS Office software – Word, Excel and PowerPoint is preferredAttention to detail and meticulous documentation practiceAutonomous clinical critical thinking abilityWhy join UHN?Competitive offer packagesGovernment organization and a member of the Healthcare of Ontario Pension Plan (HOOPP access to Transit and UHN shuttle serviceFlexible work environmentOpportunities for development and promotions within a large organizationAdditional perks (multiple corporate discounts including: travel, restaurants, parking, phone plans, auto insurance discounts, on‑site gyms, etc.)Current UHN employees must have successfully completed their probationary period, have a good employee record along with satisfactory attendance in accordance with UHN's attendance management program, to be eligible for consideration.Please be advised that a Criminal Record Check may be required of the successful candidate. Should it be determined that any information provided by a candidate be misleading, inaccurate or incorrect, UHN reserves the right to discontinue with the consideration of their application.UHN is an equal opportunity employer committed to an inclusive recruitment process and workplace. Requests for accommodation can be made at any stage of the recruitment process. Applicants need to make their requirements known.#J-18808-Ljbffr

📌 Clinical Research Coordinator Iii (Phase 1) (Toronto)
🏢 University Health Network
📍 Toronto

Reply to this offer

Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.

Subscribe to this job alert:

Get the latest job offers by email for: clinical research coordinator iii (phase 1) (toronto) / toronto

Subscribe to this job alert:

Get the latest job offers by email for: clinical research coordinator iii (phase 1) (toronto) / toronto