Clinical Research Associate
2 weeks ago
We are seeking a skilled Research Coordinator to join our growing team at William Osler Health System. This is an exciting opportunity to work in a dynamic environment and contribute to the success of our Oncology Research Department.
About the RolePatient Screening and Recruitment: The successful candidate will be responsible for screening, recruiting, and consenting patients according to the study protocol.
Study Coordination: The Research Coordinator will assist investigators in the initiation of new research, ensure completion of eligibility requirements prior to enrollment and randomization, and facilitate and coordinate the planned cancer treatment schedule for each trial patient.
Data Collection and Reporting: The coordinator will be responsible for accurate data collection, transcription, and entry, as well as timely reporting of Adverse Events and Serious Adverse Events to study sponsors, physicians, and appropriate authorities.
Regulatory Compliance: The Research Coordinator will ensure adherence to all appropriate regulations in the conduct of research, including Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans and Health Canada's Part C, Division 5 of the Food and Drug Regulations.
Qualifications- Undergraduate certificate or Bachelor's Degree in health science or related field
- Minimum two years' experience as a Research Coordinator in a Canadian environment
- Advanced knowledge of Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans and Health Canada's Part C, Division 5 of the Food and Drug Regulations
- Certification as a Clinical Research Associate (SOCRA/ARP) or in the process of completion
William Osler Health System values inclusivity and diversity in the workplace and offers a collaborative and dynamic work environment. If you are a motivated and detail-oriented individual with a passion for research, we encourage you to apply for this exciting opportunity.
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