Clinical Trials Essentials: From ICF to Site Management

  • Author: Name
  • Level: Beginner
  • Study time: 10 hours
  • Video time: 7.5 hours
  • Exams: 2
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WHAT'S INCLUDED ?

Fundamentals of Informed Consent

Dive into the ethical and legal foundations of informed consent, understanding its importance in protecting patient rights and ensuring ethical research conduct.

Drafting and Evaluating Consent Forms

Learn the art of creating clear, concise, and comprehensive consent forms, and develop skills to evaluate their effectiveness in conveying essential information to participants.

Site Management Essentials

Gain insights into the critical role of site management in clinical trials, encompassing site selection, setup, and coordination.

Communication Skills for Clinical Researchers

Enhance your communication skills, crucial for interacting with patients, healthcare professionals, and regulatory bodies.

Regulatory Compliance and Documentation

Understand the regulatory landscape governing clinical research, focusing on compliance with laws and guidelines to ensure ethical and legal research practices.

Resource Library

Access to a wealth of resources including articles, templates, and tools for ongoing learning and application.

BENEFITS OF TAKING THIS COURSE.

Enhanced Understanding of Ethical Practices

Equip yourself with comprehensive knowledge of ethical standards in clinical research, focusing on the protection of participant rights.

Improved Site Management Skills

Develop the ability to effectively manage research sites, ensuring efficient and compliant clinical trial operations.

Effective Communication Proficiency

Gain expertise in communicating complex information clearly and effectively to various stakeholders in clinical research.

In-depth Regulatory Knowledge

Acquire a deep understanding of the regulatory environment, essential for navigating the complexities of clinical trials.

Network with Industry Professionals

Connect with experts and peers, expanding your professional network.

Stay Updated with Industry Trends

Keep up with the latest trends and changes in global regulatory landscapes.

WHAT OUR STUDENTS SAY ABOUT THIS COURSE

Brenda L.

Life-Changing Learning Experience!
     
This course was a turning point in my career. The detailed modules on informed consent and site management not only broadened my knowledge but also gave me practical tools that I apply in my role as a clinical research coordinator. Highly recommend!

Gladys H.

Top-Notch Content and Delivery!
     
I'm impressed by the quality of content and the way it was delivered. The course is comprehensive, engaging, and incredibly informative. It has significantly improved my skills in informed consent and site management, which are crucial in my day-to-day work.

Tony P.

Exceptional and Impactful!
     
As a recent graduate entering the field of clinical research, this course provided me with invaluable insights into the ethical aspects and operational management of clinical trials. The case studies were particularly helpful in understanding real-world applications

COURSES YOU MAY LIKE

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Basics of Clinical Research Coordination

Master Clinical Trial File Management at the Site for Research Success
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Foundations of the Informed Consent Process

Empowering Patients: The Foundation of Informed Consent in Clinical Research
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Fundamentals of Good Clinical Practice

Good Clinical Practice (GCP) is essential for ethical and reliable clinical research at the site. It ensures participant safety, data quality, and adherence to ethical standards.
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Management of Subject Study Visits

Efficiently managing subject visits in clinical research is crucial for success. Proper planning optimizes data collection.
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Drug Accountability and Management

Effective drug accountability and management at clinical research sites is crucial for safety and regulatory compliance.
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Preparing for Monitoring Visits

Get ready for CRA monitoring visits in clinical research! We'll help you prepare for success with essential steps to ensure a smooth visit. Let's dive in!
Created by

R. MALLE

With 10+ years of experience in various hospitals and pharmaceutical companies, Rudy has honed his expertise in multiple therapeutic areas and clinical trial phases. He has excelled in leadership roles, demonstrating a strong ability to train and guide teams effectively. His practical knowledge and commitment to excellence make him a key educator in the academy.
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