Course curriculum

    1. Lesson 1: The Role of a Clinical Research Coordinator

    2. Lesson 2: Why is Clinical Research Coordinating Important?

    3. Lesson 3: The History Of Clinical Research

    4. Lesson 4: Key Roles in Clinical Research and Their Functions

    5. Chapter 1 Quiz

    1. Lesson 1: Quick Reference Guide to Protocol Understanding

    2. Lesson 2: Start-Up Regulatory Documents

    3. Lesson 3: Communication Skills

    4. Lesson 4: Essential Documents & IRB

    5. Lesson 5: Informed Consent Process

    6. Lesson 6: Generating Source Documents for a New Clinical Study

    7. Chapter 2 Quiz

    1. Lesson 1: Time Management

    2. Lesson 2: Understanding and Avoiding Protocol Deviations in Clinical Research

    3. Lesson 3: Attention to Detail

    4. Lesson 4: Electronic Data Capture (EDC), Interactive Response Technology (IRT), eConsent, and Electronic Source (eSource) in Clinical Research

    5. Lesson 5: Data Management

    6. Lesson 6: Staying On Schedule With Patient Visits

    7. Lesson 7: Problem Solving

    8. Chapter 3 Quiz

    1. Lesson 1: Everything About Audits

    2. Lesson 2: FDA Regulations

    3. Lesson 3: ICH GCP Guidelines

    4. Lesson 4: Study Close Out

    5. Chapter 4 Quiz

    1. Lesson 1: Study Start Up

    2. Lesson 2: Enrollment Period

    3. Lesson 3: Maintenance Period

    4. Lesson 4: Close-Out Period

    1. Final Assignment

    2. Final Exam

About this course

  • $2,500.00
  • 31 lessons

4 Week Program

This is an intensive 4-week program, which includes a blend of asynchronous, and synchronous training methods.

This program provides a detailed and extensive training curriculum that includes, but is not limited to the following:
    Common Medical and Pharmacologic Terms Used in Clinical Research
    Evolution and History of Clinical Research Protection of Human Subjects in Clinical Research
    ICH Good Clinical Practice
    Therapeutic Areas in Clinical Research
    FDA/EU regulations
    IRB’s
    Informed Consent
    Research Designs and Concepts
    Site Coordination and Management
    Industry Organizations
    Career Services
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Program Director

Jenn Pages

CCRP

Clinical Research Expert 🔬 About Me: With a robust 14-year tenure in the dynamic realm of clinical research, I bring a wealth of experience and expertise to the table. My journey has been one of relentless dedication and passion for advancing healthcare through meticulous research and innovation. 👩‍🔬 Experience: Throughout my career, I've had the privilege of traversing diverse roles within clinical research. From my formative years at a prominent research site to my tenure at ICON, a global leader in clinical research, I've honed my skills across every facet of the field. Most recently, I've served as both a Project Manager and Clinical Trial Manager, orchestrating multifaceted trials with precision and excellence. 💼 Role at Clinical Research Site: One of the defining chapters of my career was spearheading a clinical research site from its inception. From laying the groundwork to establishing robust protocols and procedures, I navigated every challenge with tenacity and vision. This hands-on experience equipped me with invaluable insights into the intricacies of site management, fostering a deep appreciation for the pivotal role sites play in the research ecosystem. 🌟 Key Strengths: Proven track record in project management, driving timelines and deliverables with finesse. Exceptional leadership skills honed through years of guiding cross-functional teams to success. Comprehensive understanding of regulatory requirements and industry best practices. Adept at fostering collaborative partnerships with sponsors, CROs, and site personnel to optimize trial outcomes. Passionate advocate for patient-centric research, prioritizing safety, and ethical conduct above all else. 🎓 Teaching Philosophy: As a Program Director, my goal is to empower the next generation of clinical research professionals with practical knowledge and real-world insights. Drawing from my rich tapestry of experiences, I aim to cultivate a learning environment that fosters critical thinking, problem-solving, and a deep-seated commitment to excellence.

Discover your potential, starting today.

If you are looking to take a clinical research training course, go with the program that makes you a priority.
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