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| Job Location | Scarborough, ON |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Full Time |
Clinical Research of Ontario (CRON) is a privately-owned clinical research site dedicated to providing robust services for high-quality, patient-centric clinical studies. CRON focuses on phase I-IV clinical trials across many therapeutic areas. Our Principal Investigators (PI) and Sub Investigators (SI) are board-certified physicians with numerous years of experience. They work very closely with our Clinical Research Coordinators (CRC), who have the full knowledge and expertise of Good Clinical Practice (GCP), clinical trial processes, guidelines and regulations. Our highly-qualified team of PIs, SIs and CRCs are committed to ensuring that our practice has the greatest impact on patient safety improvement to benefit the thousands of affected patients worldwide. We are urgently seeking a Dermatologist who will work as a Principal Investigators to oversee the conduct of the trials at our site.· The best applicants must be board-certified Dermatologist in Ontario· Ensure and protect the patient’s rights, safety and walfare of research subject;· Maintain strict confidentiality of patients, employees, and company information at all times and adheres to PIPEDA Guidelines;· Be thoroughly familiar with the protocol, case report form, informed consent, source documentation, patient diary (when applicable), and study medication(s) for the assigned research study;· Adhere to GCP, ICH, PIPEDA, NIH, FDA/Health Canadas Food and Drugs Regulations and SOPs, and maintain ongoing regulatory documents;· Assist and participate in study recruitment to ensure enrollment goals are met or exceeded;· Direct and guide Research Staff on study specific tasks;· Utilize and ensure the appropriate equipment is on-site;· Perform appropriate research protocol procedures which may include, but are not limited to physical exams, medical history review and assessment, assessment of vital signs, laboratory results and adverse events;· Work with the Site Director, Sub Investigator(s) and Study Coordinator to maintain high quality and patient safety;· May perform other duties per assinged protocol requirements that are not specifically listed in this job description.Qualifications: