Switch to Calendar View

Events Calendar

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

Join over 1,000 of your colleagues back in person at SOCRA's 2023 Annual Conference! For the 32nd year, SOCRA will welcome clinical research professionals from across the world. 

This 4-day workshop will assist Research Site Coordinators, Quality Assurance Auditors, and CRAs/Monitors in improving their skills and their understanding of the roles and responsibilities of the Clinical Research Associate/Monitor.

Clinical trial project and program management incorporate a broad range of skill sets in order to plan, administer, track, evaluate and report activities and budgets involved in the health care product development process. The goal of this program is to introduce, affirm or enhance the participant’s understanding of the project management endeavor.

This program will assist clinical research professionals in improving their understanding of the clinical research site responsibilities and apply skills and strategies to execute these responsibilities.

The purpose of this workshop is to assist research professionals in understanding, developing and implementing quality management systems (QMS) in the conduct of clinical trials. 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.

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.

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

Information will be presented and discussed regarding the administration of oncology clinical trials according to regulation, guidance, policy and procedure.

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 program will assist clinical research professionals in improving their understanding of the clinical research site responsibilities and apply skills and strategies to execute these responsibilities.

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.