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Clinical research coordinators (CRCs) play a vital role in the successful execution of clinical trials. They are responsible for ensuring that studies are conducted in compliance with Good Clinical Practice (GCP) guidelines, which are essential for protecting the rights, safety, and well-being of trial participants. In this post, we will explore the importance of GCP training for CRCs, the key components of effective training programs, and how to implement these practices in

Online Training & Certification Earn your certification for protecting human research participants with this online training. PHRP includes a downloadable certificate.

By law, any person who causes dangerous goods to be transported by a public carrier must follow specific regulations and must have proof of training. In a laboratory environment, "sendout staff," those transporting dangerous goods, and those receiving dangerous goods are among the individuals requiring training. Upon completion of this course, participants will be eligible to take an online self-assessment quiz to obtain a "Dangerous Goods Shipping" training completion certif

In the fast-evolving world of clinical research, the ability to efficiently collect and manage data is crucial. Electronic Data Capture (EDC) systems have transformed how researchers gather, store, and analyze data, making the process more streamlined and reliable. This blog post will explore the ins and outs of EDC in clinical research, providing practical insights and examples to help you master this essential tool. A computer screen showcasing an electronic data capture in

In today's competitive job market, gaining practical experience is crucial for launching a successful career. Many graduates find themselves struggling to secure their first job due to a lack of real-world experience. This is where Clinterra's Externship Program comes into play. This program not only bridges the gap between education and employment but also equips participants with the skills and knowledge needed to thrive in their chosen fields. What is Clinterra's Externshi

Focuses on key topics essential to the biomedical investigator’s role and responsibilities in conducting a clinical investigation of a product regulated by the U.S. Food and Drug Administration (FDA). This role-based course covers supervision, delegation, management, reports, and communication for investigators. Biomedical Principal Investigator

This course is intended to cover the core elements of the federal Health Insurance Portability and Accountability Act (HIPAA) requirements as applicable for education and research roles.

PATIENT INTAKE FORMS Patient intake forms for clinical research are specialized questionnaires used to screen trial candidates, verify eligibility criteria, and securely collect baseline medical data. These forms are critical to the integrity of a study, ensuring researchers gather structured data while fully accounting for factors that might impact trial outcomes. Core Components of a Clinical Research Intake Form A robust intake process requires several specific categories

A structured, dual-track curriculum combining hands-on procedural competency training with foundational clinical research operations.