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X-WR-CALNAME:SOCRA
X-ORIGINAL-URL:https://socra.org
X-WR-CALDESC:Events for SOCRA
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DTSTART:20250101T000000
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BEGIN:VEVENT
DTSTART;VALUE=DATE:20261112
DTEND;VALUE=DATE:20261113
DTSTAMP:20260907T132120
CREATED:20260331T235232Z
LAST-MODIFIED:20260903T021419Z
UID:229-1794441600-1794527999@socra.org
SUMMARY:Project/Program Management - Advanced 
DESCRIPTION:Advanced Project/Program Management LIVE Workshop: Nov. 12-13\n Includes Multiple Live Events. The next is on 11/12/2026 at 9:30 AM (EST) \n\n\n\nAlready registered? Log in now.\n\n\n\n\n\n\nOverview\nSpeaker(s)\nContents (4)\n\n\n\nGoal: To equip clinical research professionals with practical project and program management tools and strategies to effectively plan\, execute\, monitor\, and lead research projects while managing risk\, finances\, contracts\, teams\, and stakeholder relationships. \nMember Rate: $645.00 \nNon-Member Rate: $695.00 \nObjective: Provide attendees with the knowledge\, tools\, and practical techniques to apply project management principles to clinical research\, including planning and tracking projects\, mitigating risk\, managing budgets and contracts\,a nd navigating team and organizational dynamics. Please contact us with any questions or concerns at education@socra.org. \nLearning Objectives: Upon completion of the workshop\, the attendee should be able to: \n\nApply core project management principles and PMI concepts to the planning\, execution\, monitoring\, and completion of clinical research projects.\nUtilize project management tools and techniques\, including Gantt charts\, SOPs\, flowcharts\, and shared calendars\, to effectively plan\, track\, and assess project progress.\nIdentify and mitigate project risks using practical risk management and risk-avoidance strategies.\nApply effective approaches to study budgeting\, financial tracking\, contract management\, and sponsor-site negotiations throughout the clinical trial lifecycle.\nImplement strategies for managing diverse leadership and organizational styles\, resolving conflict\, strengthening teams\, and improving stakeholder collaboration.\n\nPlease book your Hotel Room here: 2026 SOCRA Project Management & Monitoring/GCP Conferences – Start your reservation \nPlease contact us with any questions or concerns at education@socra.org.
URL:https://socra.org/event/project-program-management-advanced/
LOCATION:Nashville\, TN
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20261112
DTEND;VALUE=DATE:20261113
DTSTAMP:20260907T132120
CREATED:20260331T235256Z
LAST-MODIFIED:20260903T021519Z
UID:230-1794441600-1794527999@socra.org
SUMMARY:Monitoring & GCP Workshop - Advanced 
DESCRIPTION:Monitoring & GCP Compliance LIVE Workshop: Nov. 12-13\n Includes Multiple Live Events. The next is on 11/12/2026 at 9:15 AM (EST) \n\n\n\nAlready registered? Log in now.\n\n\n\n\n\n\nOverview\nContents (4)\n\n\n\nGoal: To equip clinical research professionals with the knowledge and practical skills needed to effectively conduct and support clinical trial monitoring activities in accordance with Good Clinical Practice (GCP) and regulatory requirements\, ensuring participant safety\, data integrity\, protocol compliance\, and inspection readiness. \nMember Rate: $645.00 \nNon-Member Rate: $695.00 \nObjective: To provide participants with a comprehensive understanding of clinical trial monitoring\, including regulatory requirements\, Good Clinical Practice (GCP) principles\, risk-based monitoring strategies\, and best practices for identifying and managing compliance issues to support high-quality\, inspection-ready clinical research. Please contact us with any questions or concerns at education@socra.org. \nLearning Objectives: Upon completion of the workshop\, the attendee should be able to: \n\nUnderstand the purpose of clinical trial monitoring and the regulatory requirements\nApply Good Clinical Practice principles during monitoring activities and monitor prep\nEvaluate participant safety and data integrity through monitoring practices\nDescribe risk-based monitoring approaches\nIdentify\, document\, and manage non-compliance findings\nUtilize monitoring as a key component of inspection readiness and overall quality management\n\nPlease book your Hotel Room here: 2026 SOCRA Project Management & Monitoring/GCP Conferences – Start your reservation \nPlease contact us with any questions or concerns at education@socra.org.
URL:https://socra.org/event/monitoring-gcp-workshop-advanced/
LOCATION:Nashville\, TN
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20261117
DTEND;VALUE=DATE:20261118
DTSTAMP:20260907T132120
CREATED:20260903T021748Z
LAST-MODIFIED:20260903T021748Z
UID:2198-1794873600-1794959999@socra.org
SUMMARY:FDA Clinical Trial Requirements Regulations\, Compliance and GCP Conference=
DESCRIPTION:FDA Clinical Trial Requirements Regulations\, Compliance and GCP LIVE Conference- Nov.17-18\nIncludes Multiple Live Events. The next is on 11/17/2026 at 8:30 AM (EST) \n\n\n\nAlready registered? Log in now.\n\n\n\n\n\n\nOverview\nSpeaker(s)\nContents (4)\n\n\n\nThis LIVE symposium is a distinct opportunity for Sponsor-Investigators and key research staff to receive targeted training directly from FDA\, NIH\, and research industry representatives. It will provide insight into the unique dual-role of sponsor-investigators with in-depth coverage of the applicable FDA regulations\, guidelines\, and best practices. Attendees will take away tools for designing and managing quality research studies that will produce accurate and complete data submissions. The two (2) full-day schedule allows for less disruption to clinical practice and continuing education credits (CME/CNE/SOCRA CE) apply. \nPlease contact us with any questions or concerns at education@socra.org. \nPlease book your Hotel Room here: SOCRA FDA LIVE WORKSHOP ROOM RATE \nDates:\nTuesday November 17th and Wednesday November 18th\, 2026. \nTime:\n8:30 am EST to 4:00 pm EST \n*All times in Eastern Standard Time Zone \n Registration:\n\nStandard Rate – Member Fee – $600\nStandard Rate – Non-Member Fee *- $675\n\nContinuing Education Credit:\nSOCRA designates this educational activity for a maximum of 11.75 Continuing Education Credits for SOCRA CE and Nurse CNE. SOCRA designates this live activity for a maximum of 11.75 AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity. \nAccreditation Statements:\nCME for Physicians: The Society of Clinical Research Associates is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians. \nCNE for Nurses: Society of Clinical Research Associates is accredited as a provider of nursing continuing professional development by the American Nurses Credentialing Center’s Commission on Accreditation. \nSOCRA Course Series: 700 \nPlease contact us with any \nquestions or concerns at education@socra.org.
URL:https://socra.org/event/fda-clinical-trial-requirements-regulations-compliance-and-gcp-conference-2/
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