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Do you want to offer your patients cutting-edge treatments and contribute to medical breakthroughs? If so, this course is for you! The objective of this course is to equip you with the required knowledge to set up your own clinical site for success.
We will equip medical professionals with the knowledge to set up and manage successful clinical trial sites.

As a medical professional, you play a pivotal role in advancing medical research and patient care. Clinical trials offer an opportunity to test new treatments and therapies, potentially improving health outcomes for your patients and countless others.

However, establishing a successful clinical trial site requires meticulous planning, regulatory compliance, and a deep understanding of the research process. This comprehensive course, designed specifically for doctors, nurses, and medical staff, equips you with the essential skills and knowledge to confidently navigate the clinical trial landscape.

This comprehensive course covers the 6 major topics that will guide you through all the required steps for setting up your set and being selected by CROs and pharmaceutical companies. 

Here’s why this course is crucial for you:

-Enhance Patient Care: Be at the forefront of medical breakthroughs by offering your patients access to cutting-edge treatments and therapies.

-Expand Your Expertise: Gain an in-depth understanding of clinical trial design, implementation, and regulations.

-Boost Your Practice: Attract more patients by participating in clinical trials and demonstrating your commitment to research.

-Contribute to Science: Play a vital role in developing new medications and improving healthcare practices.

-Streamline Workflows: Learn efficient strategies to manage clinical trial processes while upholding patient safety and study protocols.

KEY LEARNING OBJECTIVES

Upon completion of this course, you will be able to:

1. Analyze the opportunity you have to start working in clinical research;

2. Comprehend the infrastructure required to conduct a clinical trial;

3. Understand how to carry out feasibility studies and financial planning for clinical trials;

4. Realize the importance of using Standard Operating Procedures (SOPs) in clinical trials and create your own SOPs that fit the needs of trial;

5. Describe ways to attract and retain potential subjects for trials and how to confirm their eligibility;

6. Understand the importance of Investigator oversight, and the relationship with the CRAs;

7. Compare the difference between Real World Evidence (RWE) studies and Randomized Clinical Trials (RCTs)

By the end of this comprehensive course, you’ll be well-equipped to lead your medical facility towards a successful clinical trial site, contributing to groundbreaking research, offering cutting-edge treatment options to your patients, and making a significant impact on healthcare advancement.

WHO SHOULD ATTEND THIS GCP TRAINING?

-Persons expecting to start a career in clinical research at a site level, working with Pharmaceutical Companies or CROs.

-Medical Doctors (all specialties) and dentists, with no or little experience in clinical research

-Nurses (clinical research nurses, RNs)

-Other medical Staff (pharmacists, medical technologist or clinical laboratory scientist, Imaging professionals, radiologists, raters, etc)

-Anyone interested in pursuing a career in clinical researc (study coordinators, etc).

METHODOLOGY

-The course is self-paced e-learning

-it is clearly explained and developed by pharma professionals

-You can study at your own pace with virtual modules. Your progress is automatically saved, so you can start and stop whenever you like.

-A final exam is not needed for this course

LEARNING PATH

1. OVERVIEW

2. INFRASTRUCTURE REQUIRED TO CONDUCT A CLINICAL TRIAL

3. FEASIBILITY AND FINANCIAL PLANNING

4. DEVELOP EFFECTIVE SOPs

5. ENROLL SUBJECTS

6. MANAGE THE TRIAL

7. REAL WORLD EVIDENCE STUDIES