{"id":12606,"date":"2024-07-09T19:34:41","date_gmt":"2024-07-09T19:34:41","guid":{"rendered":"https:\/\/crtsolution.com\/?page_id=12606"},"modified":"2025-10-14T19:20:06","modified_gmt":"2025-10-14T19:20:06","slug":"training","status":"publish","type":"page","link":"https:\/\/crtsolution.com\/fr\/training\/","title":{"rendered":"Formation-CRTSolution"},"content":{"rendered":"\t\t
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\r\n \r\n Training - CTRSolution <\/span>\r\n <\/div>\r\n \t

\r\n A Comprehensive Training Program for Every Stage of Your Career<\/span> <\/p>\r\n <\/div>\r\n<\/div>\r\n\r\n\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t <\/div>\n <\/div>\n <\/div>\n <\/section>\n

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\r\n \r\n Elevate Your Research. <\/span>\r\n <\/div>\r\n \t

\r\n A Better Way to Learn. A Faster Path to Success.\n\n<\/span> <\/h3>\r\n <\/div>\r\n<\/div>\r\n\r\n\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Navigating the world of clinical research requires a clear path. Whether you’re starting your first day or looking to lead your team more effectively, our programs are designed to guide you at every step \u2014 transforming potential into proven, professional expertise.<\/p>\t\t\n\t<\/div>\n<\/div>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t <\/div>\n <\/div>\n <\/div>\n <\/section>\n

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\r\n All courses are offered in French and in English<\/span> <\/h3>\r\n <\/div>\r\n<\/div>\r\n\r\n\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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\r\n New in the Field<\/a>\r\n <\/div>\r\n
This course is designed to give hands-on practical experience to those new in the field who hold little clinical research knowledge, experience or skills. At the end of this course, the employee will receive a certificate for the course.
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\nCourse content:
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\n-The History, Structure and Functions of Clinical Research
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\n-Data Management, ICH-GCP Regulations and Review Boards
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\n-Study Participant Management (Informed Consent & Safety), Privacy of Information and Quality Control (Monitoring)
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\n-Essential Document Maintenance in compliance with Canadian and International Regulations and Quality Assurance (Audit & Inspection)
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\nTraining is conducted onsite, over a 3-day period equaling 21-hours, accommodating a maximum of 3 persons.<\/div>\r\n <\/div>\r\n
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\r\n Elective Modules for Experienced Professionals<\/a>\r\n <\/div>\r\n
This option is for any experienced or practicing professional, that holds any research position, and could benefit from the reinforcement of select topics, to sharpen their research knowledge and skills, and maximize their on-the-job application and contributions, toward improving the success rate of trials.<\/div>\r\n <\/div>\r\n
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\r\n Consultation Support<\/a>\r\n <\/div>\r\n
We provide support to your team by showing you \u201cHOW TO\u201d in whatever area of clinical research activities that you may have the need. For example, mentoring support to your junior research staff, guiding your new QA officer to set up a quality assurance program, preparing your study files for inspection, etc. Just let us know what you need and we will provide the solution!!<\/div>\r\n <\/div>\r\n
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\r\n GCP Certification<\/a>\r\n <\/div>\r\n
This interactive course offers professional training and certification in good clinical practice for those new in the field and for professionals whose certification is up for renewal.<\/div>\r\n <\/div>\r\n
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\r\n Clinical Research Course for Investigators\/Sponsor-Investigators<\/a>\r\n <\/div>\r\n
This course was designed by two highly experienced clinical research professionals (both with combined roles of senior auditor, clinical study manager, site study coordinator\/nurse, senior monitor) to give new or aspiring investigators (or even those wanting a 'refresher\u2019) concise and relevant knowledge for this very important role. It can also be offered to investigators who following a health authority inspection, had an observation of inadequate Investigator oversight.
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\nBy the end of this course, the Investigator will understand his\/her role and responsibilities (and those of his\/her team) in the conduct of a clinical study; delegation of tasks; protocol compliance; regulatory and ethical expectations; source and essential documents; safety reporting; visits from monitors, auditors and inspectors; and the dual role of sponsor-investigator.
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\nThis 2.5-hour training can be conducted onsite or remotely.<\/div>\r\n <\/div>\r\n
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\r\n Clinical Research Clerk Training<\/a>\r\n <\/div>\r\n
This 8-hour course is designed for Clinical Research Clerks who assist CRAs (example, CRAs working from home or consultants CRAs who require clerical help) in various administrative tasks (such as filing) in order to give them a general knowledge and understanding of clinical research, the sponsor master file, essential documents, and CRA visits to sites.
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\nThis training is only offered remotely.<\/div>\r\n <\/div>\r\n <\/div>\r\n\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t <\/div>\n <\/div>\n <\/div>\n <\/section>\n
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