ICG is an organization that offers training services for clinical research professionals. Created with over 75 years of combined clinical research experience, our training services can benefit existing clinical research professionals, CRCs, or people looking to break into the clinical research field. We offer tailor made corporate training, resume services as well as a CRA Academy. Click below for more information about our CRA Academy.

This comprehensive introductory course is designed specifically for current and aspiring Clinical Research Associates (CRAs) who want to build a solid foundation in the clinical research field. Participants will gain insight into the fundamental principles of clinical trials, the history of clinical research, and the role of CRAs in the drug development process.

This comprehensive class equips Clinical Research Associates (CRAs) with the essential knowledge and skills to understand the design of clinical trials. Participants will explore the foundational principles of clinical research, including study objectives, protocol development, and regulatory considerations.

This comprehensive class is designed for Clinical Research Associates (CRAs) seeking to deepen their understanding of the fundamental principles of informed consent. Participants will explore the eight essential elements of informed consent. This training equips professionals with the skills necessary to uphold the integrity of clinical trials and foster trust between researchers and participants.

In the clinical research landscape, regulatory bodies play a crucial role in ensuring the safety and efficacy of medical products. This class is designed for current and aspiring Clinical Research Associates who seek to deepen their knowledge of these essential organizations. Participants will explore the functions, guidelines, and processes of key regulatory agencies, such as the FDA, EMA, and ICH. Equip yourself with the expertise to understand the regulatory environment and enhance your effectiveness as a CRA in the ever-evolving field of clinical research

Enhance your knowledge and skills in the clinical research field with our comprehensive class on Good Clinical Practices (GCPs), monitoring guidelines, and ALCOA-C++ principles. This course is designed for Clinical Research Associates eager to deepen their understanding of regulatory requirements and ensure compliance in clinical trials. Participants will explore the intricacies of GCPs, learn effective monitoring strategies, and grasp the significance of ALCOA-C principles in data integrity. Join us to empower your professional journey and excel in the vital role of a CRA.

In this comprehensive class on Site Selection and Initiation, Clinical Research Associates (CRAs) will gain essential skills and knowledge necessary for effective site operations. Participants will delve into the strategic process of selecting appropriate clinical sites, evaluating site capabilities, and establishing successful working relationships with site staff. Through a blend of theoretical knowledge and practical applications, this course prepares CRAs to confidently initiate trials and contribute to the success of clinical research projects. This course includes a simulated site selection visit as well as a simulated site initiation visit; giving students hands-on experience.

In this comprehensive class, Clinical Research Associates (CRAs) will gain a thorough understanding of essential documents and Trial Master File (TMF) review processes. Participants will learn about the critical documentation required throughout the clinical trial lifecycle, including regulatory submissions, Clinical Study Protocols, Informed Consent Forms, and more. Emphasis will be placed on best practices for maintaining compliance and accuracy within the TMF, fostering skills needed to identify gaps and ensure completeness. CRAs will develop the expertise necessary to effectively manage and review these documents, ultimately enhancing their proficiency in supporting successful clinical trials.

This course is designed to equip aspiring and current Clinical Research Associates (CRAs) with the essential skills and knowledge needed for effective clinical trial monitoring. Participants will learn best practices for site visits, and understand regulatory requirements. Students will develop the competence to oversee trials confidently, ensuring compliance and data integrity. By the end of the course, attendees will be well-prepared to navigate the complexities of clinical trial monitoring and contribute positively to the success of clinical research initiatives. This course includes a simulated monitoring visit, giving the student hands-on experience for this essential role.

In the Data Management and Data Analysis for Clinical Research Associates course, participants will gain essential skills in handling and interpreting clinical trial data. This class covers key topics such as data collection methods, data integrity, and statistical analysis techniques tailored specifically for clinical research.

Enhance your expertise in clinical research with our comprehensive class on Safety Reporting, SUSARs, Pharmacovigilance, and Investigational Brochures (IBs). This course is designed for Clinical Research Associates seeking to deepen their understanding of safety protocols and regulatory requirements in clinical trials. Participants will gain crucial insights into the identification, reporting, and management of Suspected Unexpected Serious Adverse Reactions (SUSARs) and learn best practices in pharmacovigilance. Additionally, the curriculum covers the essential elements of Investigational Brochures, empowering CRAs to effectively convey safety information to stakeholders. Equip yourself with the knowledge and skills needed to ensure the safety and well-being of trial participants while maintaining compliance with industry standards.

In the Study Closeout course, Clinical Research Associates (CRAs) will gain essential knowledge and skills to efficiently finalize clinical trials. Participants will learn the key processes involved in study closeout, including the completion of site documentation, data reconciliation, regulatory compliance, and the importance of effective communication with stakeholders. This course equips CRAs with the tools necessary to uphold the integrity of clinical research and support seamless project closure.