Clinical-research focused content from onboarding new clinical research team members to providing professional development for advanced learners. It includes topic-focused and role-based courses for clinical researchers and covers special topics not covered in our Research Foundations base subscription.
GCP consists of basic and refresher courses that provide essential good clinical practice training for research teams involved in clinical trials.
Foundational course covering the core components of the clinical research enterprise.
CRC courses focus on key topics essential to the conduct of clinical research. They are specifically tailored to the needs of clinical research coordinators.
This role-based course covers supervision, delegation, management, reports, and communication for investigators.
Covers regulatory inspections of clinical investigators and sites, including mock inspections, 482s, 483s, warning letters, communication, and CAPA plans.
An in-depth introduction to GMP for pharmaceuticals.
*A “site” is a facility owned and/or operated by or actively affiliated with a subscribing organization where 30 or more employees, agents, or students of the organization will complete CITI Program courses in a given year. Large organizations with a high learner volume, virtual learner groups, healthcare systems, science fair organizations, and other complex organizations may be considered equivalent to multiple sites. Each site shall be required to pay a CITI Program base subscription fee. Due to the increasing trend in organizational and site mergers, we want to remind our institutions that a merger does not result in two base subscriptions becoming one, since our costs of supporting these current and future learners typically do not change. Please contact us to discuss your organizational subscription needs.
Individuals who are not affiliated with a subscribing organization can purchase courses online (learn more).
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A video-enhanced guide to compliance with the FDAAA Final Rule and NIH Policy on clinical trial disclosure.
A role-based course that provides practical know-how to effectively lead or participate on data monitoring committees.
Foundational course on how to develop, negotiate, and implement a clinical trial budget.
This course focuses on developing the knowledge and skills necessary to maintain compliance and best practices associated with clinical research billing.
Foundational course covering the core components of pharmacovigilance and materiovigilance.
Learn strategies for promoting equity, diversity, and inclusivity in clinical research participation.
Foundational course covering the essential components of medical monitoring.
These courses provide learners with key information on managing controlled substances in research settings.
This course provides training on good laboratory practice for non-clinical laboratory studies that reflects regulations and best practices established by key regulatory agencies and guidelines.