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The purpose of this workshop is to assist the participant in preparing for the CCRP certification examination through a GCP review.

The purpose of this workshop is to assist the participant in preparing for the CCRP certification examination through a GCP review.

Presents project management and risk management principles, budget development / financial management and global considerations for clinical research programs.

This 4-day virtual workshop elevates your understanding of the evolving practice of clinical research monitoring. Ideal for Research Study Coordinators seeking improved collaboration with Clinical Research Monitors and for Monitors/Auditors/Project Managers with 0-5 years of experience. 

This conference provides attendees with new information, tools, and real life examples to help participants navigate the components of quality management in clinical research - quality planning, quality control, quality assurance, and quality improvement.

This conference, jointly Sponsored with the FDA, will share information regarding clinical research regulations and GCP guidelines and discuss methods to aid the research professional in their practice.

This interactive workshop is designed to assist Site Coordinators, Research Associates, and Study Nurses in improving their skills and their understanding of the responsibilities of the Clinical Research Site.

The purpose of this workshop is to assist the participant in preparing for the CCRP certification examination through a GCP review.

Information will be presented and discussed regarding the administration of clinical trials according to FDA Regulations and International Council for Harmonisation (ICH) regarding emergency clinical research.

Tailored to align with the ANA Scope and Standards of Practice for Clinical Research Nursing, this program caters not only to current clinical research nurses but also to those considering entering this profession. Packed with valuable insights, it's a must-attend for nurses, clinical staff, and managers across educational backgrounds aiming to enhance their understanding of Clinical Research Nursing.

The purpose of this workshop is to assist the participant in preparing for the CCRP certification examination through a GCP review.

This workshop will focus on providing tools and techniques that the participants can immediately utilize to benefit their clinical research programs.

**2025 Program Agenda Now Live**

This conference provides attendees with new information, management tools, and real life examples, to help participants navigate the evolving landscape of pediatric research.

This 4-day virtual workshop elevates your understanding of the evolving practice of clinical research monitoring. Ideal for Research Study Coordinators seeking improved collaboration with Clinical Research Monitors and for Monitors/Auditors/Project Managers with 0-5 years of experience. 

Clinical research project management is an evolving practice. The purpose of this 4-day workshop is to review project management and risk management principles, budget development / financial management and global considerations for clinical research programs.

This conference, jointly Sponsored with the FDA, will share information regarding clinical research regulations and GCP guidelines and discuss methods to aid the research professional in their practice.

SOCRA is excited to offer this comprehensive two day in-person workshop where you'll gain a solid understanding of the fundamental considerations for Decentralized Clinical Trials (DCTs) and learn practical approaches to designing, administration, and implementation.

This program presents advanced concepts by industry experts involved in the research and development of safe and effective medical devices. Add on the Device Basics Preconference Workshop, designed to provide a basic regulatory overview specific to medical device and is a fundamental precursor to the Main Program.

As the field of research evolves, new ethical and regulatory challenges arise, making it essential for researchers to stay up-to-date with emerging issues. This workshop aims to provide strategies for doing just that.

Presents project management and risk management principles, budget development / financial management and global considerations for clinical research programs.

This interactive 2-day workshop will introduce participants to the fundamental concepts and current issues in the development and implementation of an effective SOP program for clinical research. 

This 4-day virtual workshop elevates your understanding of the evolving practice of clinical research monitoring. Ideal for Research Study Coordinators seeking improved collaboration with Clinical Research Monitors and for Monitors/Auditors/Project Managers with 0-5 years of experience. 

Information will be presented and discussed regarding the administration of clinical trials according to Health Canada Regulations and International Council for Harmonisation (ICH) guidelines as well as practical procedures and site / sponsor / CRO relationships.

This 3 day virtual conference provides attendees with new information, tools, and real life examples to help participants navigate the components of quality management in clinical research - quality planning, quality control, quality assurance, and quality improvement.

This conference, jointly Sponsored with the FDA, will share information regarding clinical research regulations and GCP guidelines and discuss methods to aid the research professional in their practice.

This interactive virtual workshop is designed to assist Site Coordinators, Research Associates, and Study Nurses in improving their skills and their understanding of the responsibilities of the Clinical Research Site.

This 4-day virtual workshop elevates your understanding of the evolving practice of clinical research monitoring. Ideal for Research Study Coordinators seeking improved collaboration with Clinical Research Monitors and for Monitors/Auditors/Project Managers with 0-5 years of experience.