Clinical Research Coordinator III (Nurse - Phase 1)

Universityhealthnetwork; Toronto; Sur place; CAD 87 000 - 108 000; Plein temps

Avantages offerts par ce poste

HOOPP pension

Transit access

Flexible work environment

Development opportunities

Résumé du poste

University Health Network in Toronto is seeking a Clinical Research Coordinator to manage nursing-driven patient care within the Drug Development Program's Phase I trials. You will collaborate with investigators and healthcare teams to coordinate visits, ensure protocol compliance, and support data collection.

The role requires an RN with 3+ years of experience, current Ontario RN registration, and knowledge of ICH/GCP guidelines.

Qualifications

• Registered Nurse with a minimum of 3 years experience
• Current registration with the College of Nurses of Ontario
• Strong knowledge base in Phase I Clinical Trials
• 3–5 years clinical and/or professional experience is required
• Certification in clinical research (ACRP or SOCRA) or plans to obtain
• Bachelor's degree or equivalent with licensure/registration under RHPA
• Chemotherapy certification preferred
• Ability to apply nursing process in planning and evaluating patient care
• Evidence of physical and psychosocial assessments and patient/family teaching
• Training in ICH/GCP guidelines is an asset
• Knowledge of IATA shipping regulations and basic lab procedures an asset
• Excellent organizational and time management skills
• Strong analytical and problem solving skills
• Excellent interpersonal, verbal and written communication skills
• Ability to set priorities and work independently in a dynamic environment
• Proficiency with MS Office (Word, Excel, PowerPoint)
• Attention to detail and meticulous documentation
• Autonomous clinical critical thinking

Responsabilités

• Recruitment of study participants, screening and informed consent
• Coordination of patient visit schedules and study protocol activities
• Provide clinical care and data collection/documentation per ICH/GCP and UHN policies

Connaissances

Registered Nurse

Phase I trials

Nursing process

Attention to detail

Excellent communication

Time management

MS Office

Autonomous thinking

Formation

Bachelor's degree or equivalent in nursing or health field

Chemotherapy certification (DeSouza Institute)

Outils

MS Office (Word, Excel, PowerPoint)

Description du poste

Union: Non-Union

Number of Vacancies: 1

New or Replacement Position: Replacement

Site: Princess Margaret Cancer Centre

Department: Cancer Clinical Research Unit (CCRU) Nursing

Reports to: Director, Regulated Health Professions

Salary Range: $86,678 - $108,362 Per Year

Hours: 37.5 Hours Per Week

Shifts: Monday-Friday

Status: Permanent Full-time

Closing Date: December 14, 2026

Position Summary

The 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.

Duties

• Recruitment 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.

• Registered Nurse with a minimum of 3 (three) years experience
• Current registration with the College of Nurses of Ontario
• Strong knowledge base in Phase I Clinical Trials
• At minimum 3 to 5 years clinical and/or professional experience is required
• Recognized certification in clinical research (ACRP or SOCRA) obtained or plans to work towards
• Bachelor's degree, or recognized equivalent, and current certificate of competence (licensure/registration) from a college legislated under the Regulated Health Professions Act
• Chemotherapy certification (deSouza Institute) is preferred
• 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
• Training in ICH/GCP guidelines is an asset
• Knowledge of IATA shipping regulations and basic laboratory procedures an asset
• Excellent organizational and time management skills required
• Strong analytical and problem solving skills
• 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, Excel and PowerPoint is preferred
• Attention to detail and meticulous documentation practice
• Autonomous clinical critical thinking ability

Why join UHN?

In addition to working alongside some of the most talented and inspiring healthcare professionals in the world, UHN offers a wide range of benefits, programs and perks. It is the comprehensiveness of these offerings that makes it a differentiating factor, allowing you to find value where it matters most to you, now and throughout your career at UHN.

• Competitive offer packages
• Government organization and a member of the Healthcare of Ontario Pension Plan (HOOPP https://hoopp.com/ )
• Close access to Transit and UHN shuttle service
• A flexible work environment
• Opportunities for development and promotions within a large organization
• Additional 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.

All applications must be submitted before the posting close date.

UHN uses email to communicate with selected candidates. Please ensure you check your email regularly. At University Health Network (UHN), artificial intelligence technologies may be used to assist in the screening, assessment, and selection of candidates for this position.

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.

We thank all applicants for their interest, however, only those selected for further consideration will be contacted.