{"product_id":"clinical-research-coordinator-roles-and-responsibilities-training-2026-07-18","title":"Clinical Research Coordinator Roles and Responsibilities Training","description":"\u003cp class=\"header-block-grey\"\u003eCourse Description\u003c\/p\u003e \u003cp class=\"MsoNormal\" style=\"margin-bottom: 0cm; line-height: normal;\"\u003eThis foundational course prepares clinical research coordinators (CRCs) with the essential knowledge and skills needed to navigate their roles and responsibilities across all phases of a clinical trial in accordance with Good Clinical Practice (GCP) guidelines. Participants will gain a thorough understanding of the clinical research team structure, human subject protections, informed consent, investigational product management, and the documentation and safety reporting requirements critical to trial integrity. By the end of the course, coordinators will be equipped to support regulatory compliance, engage effectively with IRBs and sponsors, maintain accurate trial records, and confidently approach audits and inspections.\u003cspan style=\"mso-ascii-font-family: Aptos; mso-fareast-font-family: 'Times New Roman'; mso-hansi-font-family: Aptos; mso-bidi-font-family: 'Times New Roman'; color: #212121; mso-font-kerning: 0pt; mso-ligatures: none;\"\u003e\u003c\/span\u003e\u003c\/p\u003e \u003cp class=\"MsoNormal\" style=\"margin-bottom: 0cm; line-height: normal;\"\u003e \u003c\/p\u003e \u003cp class=\"header-block-grey\"\u003eLearning Objectives\u003c\/p\u003e \u003cul type=\"disc\"\u003e \u003cli class=\"MsoNormal\" style=\"color: black; margin-bottom: 0cm; line-height: normal; mso-list: l0 level1 lfo1; tab-stops: list 36.0pt;\"\u003e\u003cspan style=\"mso-ascii-font-family: Aptos; mso-fareast-font-family: 'Times New Roman'; mso-hansi-font-family: Aptos; mso-bidi-font-family: 'Times New Roman'; mso-font-kerning: 0pt; mso-ligatures: none;\"\u003eDescribe Investigator and coordinator responsibilities during the course of a clinical trial and apply GCP compliance\u003c\/span\u003e\u003c\/li\u003e \u003cli class=\"MsoNormal\" style=\"color: black; margin-bottom: 0cm; line-height: normal; mso-list: l0 level1 lfo1; tab-stops: list 36.0pt;\"\u003e\u003cspan style=\"mso-ascii-font-family: Aptos; mso-fareast-font-family: 'Times New Roman'; mso-hansi-font-family: Aptos; mso-bidi-font-family: 'Times New Roman'; mso-font-kerning: 0pt; mso-ligatures: none;\"\u003eDiscuss mandatory critical interactions with Institutional Review Boards (IRBs) or Ethics Committees (ECs)\u003c\/span\u003e\u003c\/li\u003e \u003cli class=\"MsoNormal\" style=\"color: black; margin-bottom: 0cm; line-height: normal; mso-list: l0 level1 lfo1; tab-stops: list 36.0pt;\"\u003e\u003cspan style=\"mso-ascii-font-family: Aptos; mso-fareast-font-family: 'Times New Roman'; mso-hansi-font-family: Aptos; mso-bidi-font-family: 'Times New Roman'; mso-font-kerning: 0pt; mso-ligatures: none;\"\u003eRecognize critical elements of human subject protection\u003c\/span\u003e\u003c\/li\u003e \u003cli class=\"MsoNormal\" style=\"color: black; margin-bottom: 0cm; line-height: normal; mso-list: l0 level1 lfo1; tab-stops: list 36.0pt;\"\u003e\u003cspan style=\"mso-ascii-font-family: Aptos; mso-fareast-font-family: 'Times New Roman'; mso-hansi-font-family: Aptos; mso-bidi-font-family: 'Times New Roman'; mso-font-kerning: 0pt; mso-ligatures: none;\"\u003eDiscuss the requirements for investigational product management and maintenance of adequate and accurate records for research trials\u003c\/span\u003e\u003c\/li\u003e \u003cli class=\"MsoNormal\" style=\"color: black; margin-bottom: 0cm; line-height: normal; mso-list: l0 level1 lfo1; tab-stops: list 36.0pt;\"\u003e\u003cspan style=\"mso-ascii-font-family: Aptos; mso-fareast-font-family: 'Times New Roman'; mso-hansi-font-family: Aptos; mso-bidi-font-family: 'Times New Roman'; mso-font-kerning: 0pt; mso-ligatures: none;\"\u003eRecognize key requirements for patient safety management and regulatory reporting.\u003c\/span\u003e\u003c\/li\u003e \u003cli class=\"MsoNormal\" style=\"color: black; margin-bottom: 0cm; line-height: normal; mso-list: l0 level1 lfo1; tab-stops: list 36.0pt;\"\u003e\u003cspan style=\"mso-ascii-font-family: Aptos; mso-fareast-font-family: 'Times New Roman'; mso-hansi-font-family: Aptos; mso-bidi-font-family: 'Times New Roman'; mso-font-kerning: 0pt; mso-ligatures: none;\"\u003eDiscuss good documentation practices for clinical research trials\u003c\/span\u003e\u003c\/li\u003e \u003cli class=\"MsoNormal\" style=\"color: black; margin-bottom: 0cm; line-height: normal; mso-list: l0 level1 lfo1; tab-stops: list 36.0pt;\"\u003e \u003cspan style=\"mso-ascii-font-family: Aptos; mso-fareast-font-family: 'Times New Roman'; mso-hansi-font-family: Aptos; mso-bidi-font-family: 'Times New Roman'; mso-font-kerning: 0pt; mso-ligatures: none;\"\u003eExamine audit and inspection readiness\u003c\/span\u003e\u003cbr\u003e \u003c\/li\u003e \u003c\/ul\u003e \u003cp style=\"color: black;margin-bottom: 0cm;line-height: normal;\"\u003e\u003cspan style=\"mso-ascii-font-family: Aptos; mso-fareast-font-family: 'Times New Roman'; mso-hansi-font-family: Aptos; mso-bidi-font-family: 'Times New Roman'; mso-font-kerning: 0pt; mso-ligatures: none;\"\u003e\u003cmeta charset=\"utf-8\"\u003eWho Should Attend\u003c\/span\u003e\u003c\/p\u003e \u003cul type=\"disc\"\u003e \u003cli style=\"list-style-type: none;\"\u003e \u003cul type=\"disc\"\u003e \u003cli\u003eNew and Aspiring Clinical Research Coordinators\u003c\/li\u003e \u003cli\u003eClinical Principal Investigators\u003c\/li\u003e \u003cli\u003eClinical Trial Assistants, Specialists and other Team Members Supporting Sites\u003c\/li\u003e \u003c\/ul\u003e \u003c\/li\u003e \u003cli style=\"list-style-type: none;\"\u003e \u003c\/li\u003e \u003cli style=\"list-style-type: none;\"\u003eInstructor \u003cul type=\"disc\"\u003e \u003cli\u003e\u003cspan\u003eNikki Christison, B.S., C.C.R.A.,T.I.A.C.R.\u003c\/span\u003e\u003c\/li\u003e \u003c\/ul\u003e \u003cp class=\"header-block-grey\"\u003e \u003c\/p\u003e \u003c\/li\u003e \u003c\/ul\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$1,195*\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 6 hours (0.6 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#: 0778-0000-23-025-L99-P. Released: 3\/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":53375393497453,"sku":"BI17654","price":1195.0,"currency_code":"USD","in_stock":true}],"url":"https:\/\/www.barnettinternational.com\/products\/clinical-research-coordinator-roles-and-responsibilities-training-2026-07-18","provider":"Barnett International ","version":"1.0","type":"link"}