{"product_id":"becoming-a-clinical-research-investigator-roles-responsibilities-and-successful-clinical-trial-management-2026-09-16","title":"Becoming a Clinical Research Investigator: Roles, Responsibilities and Successful Clinical Trial Management","description":"\u003cp class=\"header-block-grey\"\u003eCourse Description\u003c\/p\u003e\u003cp\u003eThis web seminar has been designed for the clinical investigator seeking an understanding of their role and responsibilities in the conduct of clinical trials. We will focus on the investigator's responsibility to ensure human subject protection and data integrity in the conduct of clinical trials. Specific topic areas include: Delegation to and oversight of clinical research teams, FDA regulations and appliable guidance documents, Good Clinical Practice (GCP), ICH GCP E6 R3 requirements, adverse events, and FDA inspections and sponsor audits.\u003c\/p\u003e\u003cp class=\"header-block-grey\"\u003eLearning Objectives\u003c\/p\u003e\u003cul type=\"disc\"\u003e \u003cli\u003eDescribe the clinical investigator roles and responsibilities in the conduct of human clinical trials\u003c\/li\u003e \u003cli\u003eIdentify appropriate investigator delegation and oversight\u003c\/li\u003e \u003cli\u003eDefine GCP and ICH GCP E6 R3 requirements for clinical investigators\u003c\/li\u003e \u003cli\u003eRecognize adverse events and reporting requirements in clinical trials\u003c\/li\u003e \u003cli\u003eDefine types of FDA inspections and sponsor audits\u003c\/li\u003e \u003c\/ul\u003e\u003cp class=\"header-block-grey\"\u003eWho Should Attend\u003c\/p\u003e\u003cul type=\"disc\"\u003e \u003cli\u003eClinical Investigators\u003c\/li\u003e \u003cli\u003eSub-Investigators\u003c\/li\u003e \u003cli\u003eClinical Research Team Members wanting to better understand the clinical investigator role and responsibilities in clinical research\u003c\/li\u003e \u003c\/ul\u003e\u003cp class=\"header-block-grey\"\u003eInstructor\u003c\/p\u003e\u003cp\u003eNikki Christison, B.S., C.C.R.A.,T.I.A.C.R.\u003c\/p\u003e\u003cp\u003e\u003cspan class=\"purple-link\"\u003e\u003ca href=\"\/pages\/instructor-biographies\" title=\"Click here for complete trainer biographies\"\u003eClick here for complete trainer biographies\u003c\/a\u003e\u003c\/span\u003e\u003c\/p\u003e\u003cp class=\"header-block-grey\"\u003eRegistration Fees\u003c\/p\u003e\u003cp\u003e$735*\u003c\/p\u003e\u003cp\u003e*Includes up to 20 participants per login at a single location. All participants (up to 20) are eligible for \"Certificates of Attendance,\" and accreditation, provided that accreditation requirements are met. For groups larger than 20 or for additional logins for other locations, please call +1 781.972.5400 or toll-free in the U.S. 800.856.2556, or email customer.service@barnettinternational.com for pricing.\u003c\/p\u003e\u003cp class=\"header-block-grey\"\u003eAccreditation Information\u003c\/p\u003e\u003cp\u003eBarnett International is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education. Participants will receive 1.5 hours (0.15 CEUs) of continuing education credit for full participation, including the completion of a pre-test, post-test, and program evaluation. Barnett International will issue a receipt of completion for earned CEUs within three weeks of program completion. ACPE#: 0778-0000-23-050-L99-P. Released: 9\/23. \u003cspan class=\"bold\"\u003e\u003c\/span\u003e \u003c\/p\u003e\u003cp align=\"center\"\u003e\u003cspan class=\"bold\"\u003eHold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471.\u003c\/span\u003e\u003c\/p\u003e","brand":"Barnett International","offers":[{"title":"Commercial","offer_id":53375372460397,"sku":"BI17433","price":735.0,"currency_code":"USD","in_stock":true}],"url":"https:\/\/www.barnettinternational.com\/products\/becoming-a-clinical-research-investigator-roles-responsibilities-and-successful-clinical-trial-management-2026-09-16","provider":"Barnett International ","version":"1.0","type":"link"}