{"title":"Monitoring Oncology Clinical Trials","description":"\u003cp\u003e\u003cimg title=\"Course Description\" alt=\"Course Description\" src=\"http:\/\/www.healthtech.com\/uploadedImages\/Barnett_Educational_Services\/images\/LiveSeminars\/CourseDescription.jpg?n=8101\" border=\"0\"\u003e\u003c\/p\u003e\n\u003cp class=\"Abstract\"\u003eThis course is designed for Clinical Research Associates (CRAs) currently working in the industry who are interested in gaining knowledge about monitoring in the oncology therapeutic area. As the demand for CRAs in the oncology arena continues to grow, this course offers practical, hands-on training covering oncology-specific logistical, clinical, and ethical considerations. The application of clinical monitoring skills to oncology trials is reinforced through interactive discussions, case studies, and practice-based activities. The course content is also valuable to Project Managers and CRA Managers working in the oncology field as they seek to design feasible protocols, clinical monitoring plans, and monitoring tools adaptable to the unique requirements of these study sites and trials.\u003c\/p\u003e\n\u003cp\u003e\u003cimg title=\"Learning Objectives\" alt=\"Learning Objectives\" src=\"http:\/\/www.healthtech.com\/uploadedImages\/Barnett_Educational_Services\/images\/LiveSeminars\/LearningObjectives.jpg?n=1786\" border=\"0\"\u003e\u003c\/p\u003e\n\u003cul class=\"Abstract\"\u003e\n\u003cli\u003eManage challenges with infrastructure and delegation of authority at oncology sites\u003c\/li\u003e\n\u003cli\u003eDescribe common characteristics of Institutional Review Board (IRB) review and communications in oncology trials\u003c\/li\u003e\n\u003cli\u003eExamine approaches to facilitate decision-making at sites for dosing toxicities and dose modifications in oncology trials\u003c\/li\u003e\n\u003cli\u003eApply standardized grading criteria to adverse events in oncology studies\u003c\/li\u003e\n\u003cli\u003eUtilize appropriate oncology disease progression algorithms\u003c\/li\u003e\n\u003cli\u003eAddress common challenges in managing laboratory and biomarker samples in oncology studies\u003c\/li\u003e\n\u003cli\u003eEstablish strategies to identify and obtain appropriate source documentation at oncology sites\u003c\/li\u003e\n\u003cli\u003eDevelop plans for thorough and efficient oncology monitoring visits\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003cimg title=\"Who Should Attend\" alt=\"Who Should Attend\" src=\"http:\/\/www.healthtech.com\/uploadedImages\/Barnett_Educational_Services\/images\/LiveSeminars\/WhoShouldAttend.jpg?n=5464\" border=\"0\"\u003e\u003c\/p\u003e\n\u003cul class=\"Abstract\"\u003e\n\u003cli\u003eClinical Research Associate\u003c\/li\u003e\n\u003cli\u003eClinical Research Associate Manager\u003c\/li\u003e\n\u003cli\u003eClinical Operations and Trial Management Personnel\u003c\/li\u003e\n\u003cli\u003eProject Managers\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003cimg title=\"Instructor\" alt=\"Instructor\" src=\"http:\/\/www.healthtech.com\/uploadedImages\/Barnett_Educational_Services\/images\/LiveSeminars\/Instructor.jpg?n=4140\" border=\"0\"\u003e\u003c\/p\u003e\n\u003cp class=\"Abstract\"\u003eVanessa Laroche, B.S., CIP, CQA, C.C.R.P.\u003c\/p\u003e\n\u003cp class=\"Abstract\"\u003e\u003cb\u003e\u003ci\u003e\u003ca title=\"Click here for complete trainer biographies\" style=\"color: rgb(0, 0, 255);\" href=\"https:\/\/stage.barnettinternational.com\/instructor-biographies\"\u003eClick here for complete trainer biographies\u003c\/a\u003e\u003c\/i\u003e\u003c\/b\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cimg title=\"Course Outline\" alt=\"Course Outline\" src=\"http:\/\/www.healthtech.com\/uploadedImages\/Barnett_Educational_Services\/images\/LiveSeminars\/CourseOutline.jpg?n=2216\" border=\"0\"\u003e\u003c\/p\u003e\n\u003cp class=\"Abstract\"\u003e\u003cb\u003e\u003ci\u003eDay 1: 8:30 a.m. – 5:00 p.m.\u003c\/i\u003e\u003c\/b\u003e\u003c\/p\u003e\n\u003cul class=\"Abstract\"\u003e\n\u003cli\u003e\u003cb\u003eOncology Sites and Infrastructure for Monitors\u003c\/b\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cb\u003eEthical Considerations in Oncology Clinical Trial Monitoring\u003c\/b\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cb\u003eManaging Investigational Products and Dosing in Oncology Clinical Trials\u003c\/b\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cb\u003eAdverse Event Management and Reporting in Oncology Clinical Trials\u003c\/b\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp class=\"Abstract\"\u003e\u003cb\u003e\u003ci\u003eDay 2: 8:30 a.m. – 5:00 p.m.\u003c\/i\u003e\u003c\/b\u003e\u003c\/p\u003e\n\u003cul class=\"Abstract\"\u003e\n\u003cli\u003e\u003cb\u003eTumor and Disease Progression Assessments for Monitors\u003c\/b\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cb\u003eLaboratory and Biomarker Management for Monitors\u003c\/b\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cb\u003eSource Data Verification in Oncology Clinical Trials\u003c\/b\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cb\u003eMonitoring Tools and Best Practices in Oncology Clinical Trials\u003c\/b\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003cimg title=\"Interactive Activities\" alt=\"Interactive Activities\" src=\"http:\/\/www.healthtech.com\/uploadedImages\/Barnett_Educational_Services\/images\/LiveSeminars\/InteractiveActivities.jpg?n=4477\" border=\"0\"\u003e\u003c\/p\u003e\n\u003cul class=\"Abstract\"\u003e\n\u003cli\u003eScenario: Managing the Complexity of Oncology Site Infrastructure\u003c\/li\u003e\n\u003cli\u003eCase Studies in Oncology Dosing Toxicity Management\u003c\/li\u003e\n\u003cli\u003eActivity: Identification and Toxicity Grading of Adverse Events\u003c\/li\u003e\n\u003cli\u003eSimulation: Tumor\/Disease Progression\u003c\/li\u003e\n\u003cli\u003eCritique: Adequate and Complete Source Documentation\u003c\/li\u003e\n\u003cli\u003eScenario: Planning the Monitoring Visit\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003cimg title=\"Registration Fees\" alt=\"Registration Fees\" src=\"http:\/\/www.healthtech.com\/uploadedImages\/Barnett_Educational_Services\/images\/LiveSeminars\/RegistrationFees.jpg?n=6142\" border=\"0\"\u003e\u003c\/p\u003e\n\u003cp class=\"Abstract\"\u003eRegistration fees include assorted breakfast items that will be available each day ½ hour prior to the start of the seminar. Also included is a Networking Lunch that will be served each training day.\u003c\/p\u003e\n\u003cp class=\"Abstract\"\u003eSpecial rates are available for multiple attendees from the same organization. Contact Melissa Dolen at 781-972-5418 to discuss your options and take advantage of the savings.\u003c\/p\u003e\n\u003cp class=\"Abstract\"\u003e\u003cb\u003e\u003ci\u003e\u003ca title=\"Click here for our seminar cancellation policy\" href=\"https:\/\/stage.barnettinternational.com\/EducationalServices\/SeminarFAQs.aspx\" style=\"color: rgb(0, 0, 255);\"\u003eClick here for our seminar cancellation policy\u003c\/a\u003e\u003c\/i\u003e\u003c\/b\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cimg title=\"Accreditation Information\" alt=\"Accreditation Information\" src=\"http:\/\/www.healthtech.com\/uploadedImages\/Barnett_Educational_Services\/images\/LiveSeminars\/AccreditationInformation.jpg?n=7031\" border=\"0\"\u003e\u003c\/p\u003e\n\u003cp class=\"Abstract\"\u003e\u003cimg title=\"ACPE Logo\" alt=\"ACPE Logo\" src=\"http:\/\/www.healthtech.com\/uploadedImages\/Barnett_Educational_Services_-_Under_Construction\/ACPE%20Logo.JPG\" border=\"0\"\u003eBarnett International is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education. Participants will receive 15 hours (1.5 CEUs) of continuing education credit for full participation, including the completion of a pre-test, post-test and program evaluation. Barnett International will mail ACPE statements within three weeks of program completion. ACPE# \u003cmeta charset=\"utf-8\"\u003e\u003cspan\u003e0778-0000-26-018-L99-P\u003c\/span\u003e Released: 7\/26.\u003c\/p\u003e\n\u003cp align=\"center\" style=\"color: rgb(0, 0, 255);\"\u003e\u003cb\u003e\u003ci\u003eHold this course at your company!\u003c\/i\u003e\u003c\/b\u003e\u003c\/p\u003e\n\u003cp align=\"center\" style=\"color: rgb(0, 0, 255);\"\u003e\u003cb\u003e\u003ci\u003eFor more information, contact Naila Ganatra at (215) 413-2471.\u003c\/i\u003e\u003c\/b\u003e\u003c\/p\u003e","products":[{"product_id":"monitoring-oncology-clinical-trials-2027-01-22","title":"Monitoring Oncology Clinical Trials","description":"\u003cp\u003e \u003c\/p\u003e\n\u003cp class=\"header-block-grey\"\u003eCourse Description\u003c\/p\u003e\n\u003cp\u003eThis web seminar will provide attendees with a general overview of oncology clinical trials and their distinct characteristics. We will review how oncology clinical trials differ from those in other therapeutic areas, with a special emphasis on the unique challenges of monitoring oncology clinical trials. Distinctions will be drawn between early and later phase trials. Attention will be paid to Adverse Event (AE) and Serious Adverse Event (SAE) reporting. All aspects of oncology clinical trials and how to successfully monitor them will also be discussed.\u003c\/p\u003e\n\u003cp class=\"header-block-grey\"\u003eLearning Objectives\u003c\/p\u003e\n\u003cul type=\"disc\"\u003e\n\u003cli\u003eIdentify the differences between monitoring oncology early phase clinical trials vs. later phase clinical trials\u003c\/li\u003e\n\u003cli\u003eIdentify ways in which oncology clinical trials differ from those in other therapeutic areas\u003c\/li\u003e\n\u003cli\u003eDescribe the complexities of AE and SAE monitoring in oncology clinical trials\u003c\/li\u003e\n\u003cli\u003eUtilize Common Terminology Criteria for Adverse Events (CTCAE) grading and apply CTCAE to AE source data\u003c\/li\u003e\n\u003cli\u003eDescribe the common challenges in monitoring and apply tools and techniques to overcome them\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp class=\"header-block-grey\"\u003eWho Should Attend\u003c\/p\u003e\n\u003cul type=\"disc\"\u003e\n\u003cli\u003eMonitors who are new to or are interested in learning more about oncology clinical trials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp class=\"header-block-grey\"\u003eInstructor\u003c\/p\u003e\n\u003cp\u003eVanessa Laroche, B.S., CIP, CQA, C.C.R.P.\u003c\/p\u003e\n\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\n\u003cp class=\"header-block-grey\"\u003eRegistration Fees\u003c\/p\u003e\n\u003cp\u003e$735*\u003c\/p\u003e\n\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\n\u003cp class=\"header-block-grey\"\u003eAccreditation Information\u003c\/p\u003e\n\u003cp\u003eBarnett International is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education. Participants will receive 2 hours (0.2 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. \u003cmeta charset=\"utf-8\"\u003eACPE# \u003cmeta charset=\"utf-8\"\u003e\u003cspan\u003e0778-0000-26-018-L99-P\u003c\/span\u003e Released: 7\/26.\u003c\/p\u003e\n\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":53474485240173,"sku":"BI17637","price":735.0,"currency_code":"USD","in_stock":true}]}],"url":"https:\/\/www.barnettinternational.com\/collections\/monitoring-oncology-clinical-trials.oembed","provider":"Barnett International ","version":"1.0","type":"link"}