BEGIN:VCALENDAR VERSION:2.0 PRODID:-//132.216.98.100//NONSGML kigkonsult.se iCalcreator 2.20.4// BEGIN:VEVENT UID:20260729T063127EDT-8592hL2juk@132.216.98.100 DTSTAMP:20260729T103127Z DESCRIPTION:The Clinical & Regulatory Affairs Experience (C&RA Experience) Training Program: A part-time clinical and regulatory affairs training pro gram exclusively for current graduate students or postdoctoral fellows.  T he C&RA Experience training program involves theoretical learning and a pr actical externship in the clinical trials environment to provide: https:// www.youtube.com/watch?v=l5BRRkDyVqA Knowledge of drug development\, clinic al trial design and regulatory processes relevant to the management and op erations of clinical trialsAwareness of the different roles of the clinica l and regulatory affairs teamTraining in essential skills (hard and soft) that are required for a career in the industry.Hands-on experience in clin ical and regulatory affairs in the context of clinical trials. [For 91ºÚÁÏÍø trainees only] Info Session for the C&RA Experience: Thursday\, September 23rd @ 12 – 12:30 pm. Learn more about the program and application requir ements. The session will be recorded\, registered participants will receiv e a link to the recording. Note: The recording will be available as early as September 27. Register for the info session: https://www.surveymonkey.c om/r/cra_exp_info This program is aimed at preparing trainees for a career as a CRA\, CRC\, MSL\, regulatory affairs specialist\, scientific evaluat or\, and more. Some of the tangible outcomes of this program for trainees are: Completion of certifications in Good Clinical Practice (ICH) and Heal th Canada Division 5.Knowledge of the regulations and practices around cli nical research\, interventional trials\, sponsor-initiated trials\, and dr ug development for adult and pediatric patientsAccess to a network of clin ical trials professionals and past alumni of the program.Practical onsite experience in a busy academic clinical trials center (Centre for Innovativ e Medicine (CIM) of the Research Institute of the MUHC). [For 91ºÚÁÏÍø Stude nts only]  Participants to the C&RA program spend approximately 2 hours a week participating in special seminars and journal clubs (online in 2021-2 022) curated to expand their understanding of the different components of drug development and clinical research. Two formal certifications for cond ucting clinical research will be completed online. The program provides on e on one career advising to trainees as they discover more about different roles and aspects of the clinical and regulatory affairs sub-sector. Subs tantial time will be spent on learning about activities associated with co nducting clinical trials and clinical research.   IMPORTANT DATES (2021-20 22)Applications open: September 27\, 9:00 EST - October 4\, 23:59 EST | Li nk for applications: https://www.surveymonkey.com/r/cra_expReview of appli cations: October 4 - 8Interview period: October 12 - 22Final decision: Wee k of October 25Expected start of the program: November 2021Expected comple tion of the program: May 2022Online Event InstructionsA link will be share d with registered participants the day before. DTSTART:20210923T160000Z DTEND:20210923T163000Z SUMMARY:Clinical and Regulatory Affairs Training Program Information Sessio n URL:/involvement/channels/event/clinical-and-regulator y-affairs-training-program-information-session-333286 END:VEVENT END:VCALENDAR