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X-WR-CALNAME:SOCRA
X-ORIGINAL-URL:https://socra.org
X-WR-CALDESC:Events for SOCRA
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TZID:UTC
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TZOFFSETFROM:+0000
TZOFFSETTO:+0000
TZNAME:UTC
DTSTART:20250101T000000
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BEGIN:VEVENT
DTSTART;VALUE=DATE:20260616
DTEND;VALUE=DATE:20260617
DTSTAMP:20260907T170439
CREATED:20260331T234601Z
LAST-MODIFIED:20260331T235456Z
UID:221-1781568000-1781654399@socra.org
SUMMARY:CCRP Prep and GCP Review Course
DESCRIPTION:
URL:https://socra.org/event/ccrp-prep-and-gcp-review-course-3/
LOCATION:Virtual 
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260609
DTEND;VALUE=DATE:20260610
DTSTAMP:20260907T170439
CREATED:20260331T234439Z
LAST-MODIFIED:20260331T234450Z
UID:220-1780963200-1781049599@socra.org
SUMMARY:Monitoring & GCP Workshop - Beginner
DESCRIPTION:
URL:https://socra.org/event/monitoring-gcp-workshop-beginner/
LOCATION:Virtual 
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260520
DTEND;VALUE=DATE:20260522
DTSTAMP:20260907T170439
CREATED:20260331T234349Z
LAST-MODIFIED:20260401T205942Z
UID:219-1779235200-1779407999@socra.org
SUMMARY:Project Management - Beginner 
DESCRIPTION:Goal\nThis introduction to clinical research project management workshop incorporates a broad range of skill sets in order to plan\, administer\, track\, evaluate and report on activities involved clinical research process. The goal of this interactive workshop is to introduce\, affirm\, and enhance the participant’s understanding of project management. \nObjective\nThrough discussion\, presentation\, and interaction\, this virtual program will broaden the participants’ knowledge of the project management art and science. Please contact us with any questions or concerns at education@socra.org. \nLearning Objectives\nUpon completion of the workshop\, the attendee should be able to: \n\nDescribe  skills and responsibilities to move from a clinical research coordinator or other research roles to learn about the responsibilities of a Project Manager.\nDefine key terms and concepts associated with Project Management.\nDescribe project management processes following PMI (Project Management Institute) guidelines (initiation\, planning\, execution\, monitoring\, controlling\, and closing).\nDiscuss the processes and procedures that are necessary to develop an infrastructure that will support the various tasks associated with Project Management in Clinical Research.\nDescribe Project Management constraints including Scope\, Time\, Budget\, and Performance.\nLearn about effective strategies in Virtual Project Management and Decentralized Clinical Trials.\nDiscuss basic principles of Risk Management\, Risk Avoidance and Risk Mitigation.\nLearn how Organizational Tools and Techniques can improve effectiveness and maintain quality in project management.\nDiscuss Organizational Dynamics and self-management in project management to promote effective team building.\nDiscuss approaches to work effectively with different leadership styles and organizational cultures.\n\nPlease contact us with any questions or concerns at education@socra.org.
URL:https://socra.org/event/project-management-beginner/
LOCATION:Virtual 
ATTACH;FMTTYPE=image/png:https://socra.org/wp-content/uploads/2026/03/SOCRA_events_featured4-1.png
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260508
DTEND;VALUE=DATE:20260509
DTSTAMP:20260907T170439
CREATED:20260331T234215Z
LAST-MODIFIED:20260401T205724Z
UID:218-1778198400-1778284799@socra.org
SUMMARY:Pediatric Clinical Trials
DESCRIPTION:This interactive virtual workshop will be facilitated by clinical research professionals with a wealth of industry expertise. The purpose of this workshop is to assist research professionals in improving their skills and their understanding of the responsibilities of conducting clinical research in the pediatric population. This conference provides attendees with new information\, management tools\, and real life examples\, to help participants navigate the evolving landscape of pediatric research. \nContinuing Education Credit Hours\nSOCRA designates this educational activity for a maximum of 6.5 Continuing Education Credits for SOCRA CE and Nurse CNE. SOCRA designates this live activity for a maximum of 6.5 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 continuing nursing education by the American Nurses Credentialing Center’s Commission on Accreditation. \nSOCRA Course Series: 850
URL:https://socra.org/event/pediatric-clinical-trials/
LOCATION:Virtual 
ATTACH;FMTTYPE=image/png:https://socra.org/wp-content/uploads/2026/03/SOCRA_events_featured2.png
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260428
DTEND;VALUE=DATE:20260430
DTSTAMP:20260907T170439
CREATED:20260331T233814Z
LAST-MODIFIED:20260401T203613Z
UID:216-1777334400-1777507199@socra.org
SUMMARY:FDA Clinical Trial Requirements Regulations\, Compliance and GCP Conference
DESCRIPTION:This virtual 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 note\, this workshop is intended to be interactive. Video attendance is strongly encouraged. Once you register\, you will be able to install and test the appropriate software to ensure your audio and video will work properly during the program. Please be sure to give yourself time to address any technical issues that might arise. Please contact us with any questions or concerns at education@socra.org. \nContinuing Education Credit Hours:\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
URL:https://socra.org/event/fda-clinical-trial-requirements-regulations-compliance-and-gcp-conference/
LOCATION:Virtual 
ATTACH;FMTTYPE=image/png:https://socra.org/wp-content/uploads/2026/03/SOCRA_events_featured1.png
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20260422
DTEND;VALUE=DATE:20260424
DTSTAMP:20260907T170439
CREATED:20260331T233432Z
LAST-MODIFIED:20260401T205846Z
UID:214-1776816000-1776988799@socra.org
SUMMARY:CCRP Prep and GCP Review Course
DESCRIPTION:Goal\nThe purpose of this workshop is to assist the participant in preparing for the CCRP certification examination. \nThis course will review the concepts identified in the CCRP Certification Examination Content Outline\, as well as the Standards of Practice including the ICH Guidelines and FDA Regulations that govern clinical research practice. \nObjective\nThe goal will be accomplished through lecture\, discussion and practical application facilitated by certified clinical research professionals with combined clinical research experience of more than 20 years. Information will be presented and discussed regarding the conduct of clinical trials; regulatory guidelines regarding IRB oversight and human research protections; ethical issues in clinical research; and workshops will stress the ability to follow directions and practices related to abstracting information and completing case report forms and other records. \nLearning Objectives\nUpon completion of the workshop\, the attendee should be able to: \nDiscuss the basic requirements necessary to meet the demands of a CRP in clinical practice\nDiscuss the basic components of compliance – Law\, regulation\, guidance\, policy and procedure\nExplain the drug/biologic development process\nDescribe the device development process\nOutline concepts for Good Clinical Practice (GCP)\nExplain the elements of informed consent\nDescribe the membership and reporting requirements of IRBs\nExplain rules relating to financial disclosure\nDiscuss the basics of study design\nExplain the rules and reporting requirements for adverse events and serious adverse events\nExplain study closure procedures and record retention guidelines\nOutline the reasons for monitoring\, audits and site visits\nExplain the Food and Drug Administration rules\, regulations\, and guidelines on research\nDiscuss the importance of investigational drug accountability\nDemonstrate and describe how to read clinical reports and records\nDiscuss Quality Assurance including\, Monitoring and Auditing\nExplain issues that would constitute clinical fraud \nThe purchase of this course is optional. It is not required to sit for or pass the CCRP certification exam. Purchasing and completing this course will not guarantee a passing score on the CCRP certification examination.
URL:https://socra.org/event/ccrp-prep-and-gcp-review-course-2/
LOCATION:Virtual 
ATTACH;FMTTYPE=image/png:https://socra.org/wp-content/uploads/2026/03/SOCRA_events_featured3.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20260225T000000
DTEND;TZID=UTC:20260226T000000
DTSTAMP:20260907T170439
CREATED:20260331T232944Z
LAST-MODIFIED:20260331T233837Z
UID:209-1771977600-1772064000@socra.org
SUMMARY:CCRP Prep and GCP Review Course 
DESCRIPTION:
URL:https://socra.org/event/ccrp-prep-and-gcp-review-course/
LOCATION:Virtual 
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