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Clinical Research Coordinator III (Research Nurse)

Employer
University Health Network
Location
Toronto, Ontario
Closing date
Sep 29, 2022

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Clinical Research Coordinator III (Research Nurse) - Toronto, Ontario

Job Posting #900157 Position: Clinical Research Coordinator III (Research Nurse) Site: Princess Margaret Hospital Department: Department of Medical Oncology Reports to: Nurse Manager, Clinical Trials DMOH, Principal Investigator Pay Range: $76,440 - $95,550 per annum (Commensurate with experience and consistent with UHN Compensation Policy) Hours: 37.5 per week Status: Permanent Full-time University Health Network (UHN) is looking for an experienced professional to fill the key role of Clinical Research Coordinator III in our Medical Oncology Department. Transforming lives and communities through excellence in care, discovery and learning. The University Health Network , where "above all else the needs of patients come first" , encompasses Toronto Rehabilitation Institute, Toronto General Hospital, Toronto Western Hospital, Princess Margaret Cancer Centre and the Michener Institute of Education at UHN. The breadth of research, the complexity of the cases treated, and the magnitude of its educational enterprise has made UHN a national and international resource for patient care, research and education. With a long tradition of groundbreaking firsts and a purpose of "Transforming lives and communities through excellence in care, discovery and learning" , the University Health Network (UHN), Canada's largest research teaching hospital, brings together over 16,000 employees, more than 1,200 physicians, 8,000+ students, and many volunteers. UHN is a caring, creative place where amazing people are amazing the world. University Health Network (UHN) is a research hospital affiliated with the University of Toronto and a member of the Toronto Academic Health Science Network. The scope of research and complexity of cases at UHN have made it a national and international source for discovery, education and patient care. Research across UHN's five research institutes spans the full spectrum of diseases and disciplines, including cancer, cardiovascular sciences, transplantation, neural and sensory sciences, musculoskeletal health, rehabilitation sciences, and community and population health.Find out about our purpose, values and principles here. (https://www.uhn.ca/corporate/AboutUHN/Purpose\Performance/Pages/purpose\values_principles.aspx) The Clinical Research Coordinator III collaborates with Investigators and health care team to assume responsibility for the overall patient management and coordination of several clinical studies for the Department of Medical Oncology at Princess Margaret Hospital. The research nurse will work primarily with the Multiple Myeloma disease site group. Studies include pharma-sponsored, cooperative group sponsored (such as NCIC) as well as Investigator initiated trials. Responsibilities include 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),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. The Clinical Research Coordinator III identifies, analyzes and interprets research participant and/or trial information and uses sound knowledge, skill and judgment to respond proactively and/or in a timely manner. QUALIFICATIONS - Registered Nurse with a minimum of three (3) years' experience. - Current registration with the College of Nurses of Ontario in good standing - Minimum one (1) year clinical experience in oncology - 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 - Demonstrated knowledge and ability to utilize the nursing process in assessing, planning, implementing and evaluating patient care - Evidence of strong physical assessment, psychosocial assessment and patient/family teaching skills - Autonomous clinical critical thinking ability - Strong knowledge base of Multiple Myeloma and CLL - BScN preferred - Recognized certification in clinical research (ACRP or SOCRA) obtained or plan to work towards - CNA certification in Oncology and/or Palliative Care or defined plan to work towards - Previous clinical research experience preferred - Training in ICH/GCP guidelines an asset. - Knowledge of IATA shipping regulations and basic laboratory procedures an asset - deSouza Chemo certification an asset - Proficiency with MS Office software Word, Excel and PowerPoint preferred. If you are interested in making your contribution at UHN, please apply on-line. You will be asked to copy and paste as well as attach your resume and covering letter. You will also be required to complete some initial screening questions. Posted: June 2, 2022 Closing Date: Until Filled For current UHN employees, only those who have successfully completed their probationary period, have a good employee record along with satisfactory attendance in accordance with UHN's attendance management program, and possess all the required experience and qualifications should apply. UHN thanks all applicants, however, only those selected for an interview will be contacted. UHN is a respectful, caring, and inclusive workplace. We are committed to championing accessibility, diversity and equal opportunity and welcomes all applicants including but not limited to: all religions and ethnicities, LGBTQ2s+, BIPOC, persons with disabilities and all others who may contribute to the further diversification of ideas. Requests for accommodation can be made at any stage of the recruitment process providing the applicant has met the Bona-fide requirements for the open position. Applicants need to make their requirements known when contacted.

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