BEGIN:VCALENDAR VERSION:2.0 PRODID:-//132.216.98.100//NONSGML kigkonsult.se iCalcreator 2.20.4// BEGIN:VEVENT UID:20260729T062708EDT-3478uz3tF2@132.216.98.100 DTSTAMP:20260729T102708Z DESCRIPTION:The Clinical & Regulatory Affairs Experience (C&RA Experience) Training Program: A part-time clinical and regulatory affairs training pro gram\, offered by the Research Institute of the MUHC\, exclusively for cur rent graduate students or postdoctoral fellows. ARE YOU LOOKING TO BUILD A CAREER IN CLINICAL AND REGULATORY AFFAIRS AS A SCIENTIST IN DRUG DEVELOPM ENT\, CLINICAL RESEARCH ASSOCIATE\, REGULATORY AFFAIRS SPECIALIST\, SCIENT IFIC EVALUATOR\, OR MEDICAL SCIENCE LIAISON? Learn more about the program and application requirements: Information sessions about the C&RA Experien ce training program will be held on: Wednesday\, August 31st\, 9:30am (onl ine)Friday\, September 16th at 12pm (online) Register for the info session : https://www.surveymonkey.com/r/cra_info_2022https://www.youtube.com/watc h?v=l5BRRkDyVqA&t=5s About this program                                                                 The C&RA Experience training program is accep ting applications from health research trainees currently enrolled as a gr aduate student (MSc or PhD) or postdoc who would like to learn about: Drug development\,Clinical trial design and regulatory processes\,Management a nd operations of clinical trials.              Careers in clinical and reg ulatory affairs. And who would like to:               Build their skillset s (hard and soft) for a career in the industry.                              Gain hands-on experience developed through case-studies\, group exercise s\, job simulations and shadowing carried out in clinical trials environme nts [shadowing is for 91ºÚÁÏÍø Students only]     Some of the concrete outco mes of this program for trainees are:                                         Completion of certifications in Good Clinical Practice (ICH) and Health Canada Division 5.Knowledge of the regulations and practices around clini cal research\, interventional trials\, sponsor-initiated trials\, and drug development for adult and pediatric patients.Access to a network of clini cal trials professionals\, mentors and past alumni of the program.Exposure to a busy academic clinical trials centre (Centre for Innovative Medicine (CIM) of the Research Institute of the MUHC). [for 91ºÚÁÏÍø students only]  More information about the program: Trainees in the C&RA program spend app roximately 2 hours a week participating in online seminars designed to exp and their knowledge of clinical research\, clinical trials and associated careers. Participants will complete two formal clinical research certifica tions. In addition\, trainees will have access to one-on-one career advisi ng with a certified career educator. New this year\, the trainees in the p rogram will participate in case-studies\, group exercises and job simulati ons where they will receive feedback from mentors. If conditions allow\, s tudents from 91ºÚÁÏÍø will shadow employees in a clinical trials environment. This program is aimed at preparing trainees for a career as a scientist in industry\, CRA\, CRC\, MSL\, regulatory affairs specialist\, scientific evaluator\, and more. Applications are competitive and spaces are limited. The application period is from September 26 – October 4\, 202 2.Online Event InstructionsA link will be sent to registered participants of the info session. DTSTART:20220831T133000Z DTEND:20220831T141500Z SUMMARY:Clinical and Regulatory Affairs Training Program Information Sessio n URL:/involvement/channels/event/clinical-and-regulator y-affairs-training-program-information-session-340968 END:VEVENT END:VCALENDAR