Clinical Study and Regulatory Specialist I - Toronto, OntarioJOB TITLE: Clinical Study and Regulatory Specialist I

　　Job Posting #: 928030

　　Site: Princess Margaret Cancer CentreDepartment: Division of Medical Oncology and Hematology Clinical Trials Group

　　Reports to: Clinical Research Manager, DMOH-CTGHours: 37.5 hours per weekSalary: $64,974 $81,218 annually: To commensurate with experience and consistent with UHN compensation policy

　　Status: Permanent Full TimePosted Date: January 16, 2024 (repost)

　　Closing Date: February 16, 2024

　　The University Health Network, where “above all else the needs of patients come first”, encompasses Toronto General Hospital, Toronto Western Hospital, Princess Margaret Cancer Centre, Toronto Rehabilitation Institute and the Michener Institute of Education. 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 ground breaking 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.

　　Position Summary & DutiesThe Clinical Study and Regulatory Specialist I participates in the coordination of clinical trials from protocol activation and follow up to trial closure. Principal responsibilities include monitoring and promoting the quality and integrity of data, recording clinical trial data in case report forms (CRFs), and compilation of ethics and regulatory documents. The coordination and monitoring of data is performed in accordance with the trial protocol, hospital and departmental guidelines and professional standards of practice. Data is assessed, compiled, recorded and submitted to pharmaceutical companies or used for internal studies. All data must be complete, accurate, timely and must be in compliance with applicable ICH-GCP, FDA and US federal code and Tri-Council regulations. The Clinical Study and Regulatory Specialist I must be able to interpret the applicable regulations in order to ensure compliance. Quality assurance procedures are utilized to ensure high quality data is obtained.

　　QualificationsAt minimum, a completion of a Bachelor’s degree program, or recognized equivalent in Health or Science-Related Discipline

　　At least two (2) year experience in some or all of Oncology, Clinical trials, medical terminology, regulatory issues involving human subjects

　　At least one (1) year experience in the review and preparation of Health Canada and Research Ethics Board submissions, including writing informed consent forms

　　Demonstrated relevant clinical research knowledge

　　Excellent written and verbal communication skills, excellent organization, prioritization skills, good computer skills, ability to learn quickly and work independently

　　Excellent interpersonal skills

　　Ability to work under pressure and attention to detail

　　Ability to perform duties in a professional and courteous manner and produce high quality work while meeting deadlines in accordance to UHN standards

　　Ability to perform multiple concurrent tasks

　　Knowledge of applicable legislative, UHN and/or departmental policies

　　Client service oriented, with the ability to effectively work with diversity and appreciate that people with different opinions, backgrounds and characteristics bring richness to the challenge or situation at hand

　　Satisfactory attendance

　　Certification as a Clinical Research Professional, preferred

　　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.

　　Vaccines (COVID and others) are a requirement of the job unless you have an exemption on a medical ground pursuant to the Ontario Human Rights Code.

　　UHN is a respectful, caring, and inclusive workplace. We are committed to championing accessibility, diversity and equal opportunity. Requests for accommodation can be made at any stage of the recruitment process. Applicants need to make their requirements known in advance. Any information received related to an accommodation will be addressed confidentially.

　　University Health Network thanks all applicants, however, only those selected for an interview will be contacted.