Clinical Research Coordinators (CRCs)

CRA Relationships with CRCs

Clinical research associates (CRAs) and clinical research coordinators (CRCs) play critical roles in the success of any clinical trial. This webinar explores their functions in...

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CRAs and Interim Monitoring Visits

The Clinical Research Associate’s (CRA) duties are to ensure that the clinical trial is conducted according to the protocol, good clinical practice, and other applicable...

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From Protocol to Manual of Procedures (MOP)

A manual of procedures (MOP) can play an important role in the conduct of a clinical trial. Unlike a protocol, which can leave out the...

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Discrete Choice Experiments with Neurologic Disorders

This webinar explores the design and execution of discrete choice experiments (DCEs) that focused on pediatric epilepsy and critical trade-offs in decision-making for neurotechnological interventions....

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Clinical Trial Staff Diversity and Cultural Humility

Increasing diversity among trial subjects helps ensure the generalizability of research findings. Leveraging clinical trial staff diversity and using cultural humility for self-reflection in recruitment...

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CRA Soft Skills, Time Management, and Effective Site Relationships

The job of a clinical research associate (CRA) involves managing the relationships they have with sites and sponsors. As a result, it is critical that...

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Improving the Clinical Trial Participant’s Experience: From Recruitment through Study Closure

The webinar examines strategies that sites, sponsors, and clinical research organizations (CROs) can use to improve participants’ experience in clinical trials. The webinar discusses this...

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ClinicalTrials.gov Enforcement: An Update

Recently, there have been updates to ClinicalTrials.gov enforcement and various initiatives to drive transparency. Institutions are challenged to build robust compliance programs and individuals must...

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Building a ClinicalTrials.gov Compliance Program – Tips for Investigators and Institutions

This webinar covers a brief overview of the regulations, important timelines to follow, agency-specific variances, and a range of compliance mechanisms. It also covers the...

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Informed Consent and Clinical Investigations: A Focus on the Process

This webinar discusses how to improve the informed consent process for subjects enrolling in clinical research. It focuses on the process used to deliver information...

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