{"product_id":"monitoring-oncology-clinical-trials-2026-10-23","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 \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 \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 \u003cul class=\"Abstract\"\u003e \u003cli\u003eManage challenges with infrastructure and delegation of authority at oncology sites \u003c\/li\u003e \u003cli\u003eDescribe common characteristics of Institutional Review Board (IRB) review and communications in oncology trials \u003c\/li\u003e \u003cli\u003eExamine approaches to facilitate decision-making at sites for dosing toxicities and dose modifications in oncology trials\u003c\/li\u003e \u003cli\u003eApply standardized grading criteria to adverse events in oncology studies\u003c\/li\u003e \u003cli\u003eUtilize appropriate oncology disease progression algorithms\u003c\/li\u003e \u003cli\u003eAddress common challenges in managing laboratory and biomarker samples in oncology studies\u003c\/li\u003e \u003cli\u003eEstablish strategies to identify and obtain appropriate source documentation at oncology sites\u003c\/li\u003e \u003cli\u003eDevelop plans for thorough and efficient oncology monitoring visits\u003c\/li\u003e \u003c\/ul\u003e \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 \u003cul class=\"Abstract\"\u003e \u003cli\u003eClinical Research Associate\u003c\/li\u003e \u003cli\u003eClinical Research Associate Manager\u003c\/li\u003e \u003cli\u003eClinical Operations and Trial Management Personnel\u003c\/li\u003e \u003cli\u003eProject Managers\u003c\/li\u003e \u003c\/ul\u003e \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 \u003cp class=\"Abstract\"\u003e\u003cb\u003e\u003ci\u003eThe course will be led by one of the following instructors:\u003c\/i\u003e\u003c\/b\u003e\u003c\/p\u003e \u003cp class=\"Abstract\"\u003eKaren L. Gilbert, B.S., C.C.R.A\u003c\/p\u003e \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 \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 \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 \u003cul class=\"Abstract\"\u003e \u003cli\u003e\u003cb\u003eOncology Sites and Infrastructure for Monitors\u003c\/b\u003e\u003c\/li\u003e \u003cli\u003e\u003cb\u003eEthical Considerations in Oncology Clinical Trial Monitoring\u003c\/b\u003e\u003c\/li\u003e \u003cli\u003e\u003cb\u003eManaging Investigational Products and Dosing in Oncology Clinical Trials\u003c\/b\u003e\u003c\/li\u003e \u003cli\u003e\u003cb\u003eAdverse Event Management and Reporting in Oncology Clinical Trials\u003c\/b\u003e\u003c\/li\u003e \u003c\/ul\u003e \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 \u003cul class=\"Abstract\"\u003e \u003cli\u003e\u003cb\u003eTumor and Disease Progression Assessments for Monitors\u003c\/b\u003e\u003c\/li\u003e \u003cli\u003e\u003cb\u003eLaboratory and Biomarker Management for Monitors\u003c\/b\u003e\u003c\/li\u003e \u003cli\u003e\u003cb\u003eSource Data Verification in Oncology Clinical Trials\u003c\/b\u003e\u003c\/li\u003e \u003cli\u003e\u003cb\u003eMonitoring Tools and Best Practices in Oncology Clinical Trials\u003c\/b\u003e\u003c\/li\u003e \u003c\/ul\u003e \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 \u003cul class=\"Abstract\"\u003e \u003cli\u003eScenario: Managing the Complexity of Oncology Site Infrastructure\u003c\/li\u003e \u003cli\u003eCase Studies in Oncology Dosing Toxicity Management\u003c\/li\u003e \u003cli\u003eActivity: Identification and Toxicity Grading of Adverse Events\u003c\/li\u003e \u003cli\u003eSimulation: Tumor\/Disease Progression \u003c\/li\u003e \u003cli\u003eCritique: Adequate and Complete Source Documentation\u003c\/li\u003e \u003cli\u003eScenario: Planning the Monitoring Visit\u003c\/li\u003e \u003c\/ul\u003e \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 \u003cp class=\"Abstract\"\u003eRegistration fees include assorted breakfast items that will be available each day 1\/2 hour prior to the start of the seminar. Also included is a Networking Lunch that will be served each training day.\u003c\/p\u003e \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 \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 \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 \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# 0778-0000-16-018-L01-P. Released: 3\/16.\u003c\/p\u003e \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 \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","brand":"Barnett International","offers":[{"title":"Commercial","offer_id":53375370232173,"sku":"BI17492","price":735.0,"currency_code":"USD","in_stock":true}],"url":"https:\/\/www.barnettinternational.com\/products\/monitoring-oncology-clinical-trials-2026-10-23","provider":"Barnett International ","version":"1.0","type":"link"}