eLearning Courses

eLearningWhen you need quality, in-depth training but are short on time and financial resources, ACRP's all-new eLearning Courses are the perfect solution.

With ACRP's eLearning Courses, you will experience in-depth, performance-based, cost-effective clinical research training in a self-paced, interactive and engaging new online format.

eLearning at ACRP is about more than just "technology" — it's about leveraging proven training methods and tools to ensure your participation results in true comprehension of course content and the ability to apply what you've learned to avoid and resolve problems and improve your job performance.

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Good Clinical Practice: An Introduction to ICH GCP Guidelines
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Good Clinical Practice: An Introduction to ICH GCP Guidelines

TransCelerate Recognized TrainingACRP's on-demand eLearning Course equips you with not only an understanding of the core concepts of Good Clinical Practice (GCP) but how to put those concepts into action through a series of ongoing "knowledge checks" and real-world scenarios likely to be encountered during a clinical trial. This course provides formal training on the International Conference on Harmonization (ICH) Guidelines for GCP, the globally recognized standard for the conduct of clinical trials, for clinical research professionals with less than 1 year of experience.

Ethics: Identifying Potential Pitfalls in Human Subject Protection
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Ethics: Identifying Potential Pitfalls in Human Subject Protection

ACRP's on-demand eLearning Course provides in-depth training on the importance of ethical conduct in clinical trials involving human subjects and how to put the rules into practice to ensure human subject safety and well-being at all times. Learn how to avoid unethical conduct in clinical trials and how to resolve issues pertaining to actual or potential unethical conduct through a thorough review of the historical evolution of ethics in clinical research, the primary guidelines involving ethical considerations in clinical research, the elements of those guidelines, and the consequences of unethical conduct and decisions.

GCP for the Experienced CRA
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GCP for the Experienced CRA: Improving Monitoring Efficiency and Effectiveness

NEW ACRP's on-demand eLearning Course improves your monitoring skills by breaking down Good Clinical Practice (GCP) into four memorable categories (Verify, Ensure, Determine and Communicate) to enable easy recall and application of the GCP E6 guideline during your work as a Clinical Research Associate (CRA). By providing you with real-world illustrations and examples of efficient, effective monitoring approaches, this course improves your monitoring skills and as a result enhances your value as a CRA.

GCP for the Experienced CRC
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GCP for the Experienced CRC: Partnering with Your Investigator to Reduce Risk and Avoid Common Inspection Findings

TransCelerate Recognized TrainingNEW ACRP's on-demand eLearning Course helps you, as a Clinical Research Coordinator (CRC), avoid today's most common inspection findings through practical, memorable application of the Good Clinical Practice (GCP) E6 guideline, and as a result reduce risk and attract more clinical trials to your Investigator's research site. By highlighting today's most common inspection findings — and providing you with best practices, illustrations and examples to avoid them through correct application of GCP guidelines — this course will better prepare you for audits/inspections and enhance your value as a CRC.

GCP for the Experienced Investigator
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GCP for the Experienced Investigator: Reducing Risks and Avoiding Common Inspection Findings

TransCelerate Recognized TrainingNEW ACRP's on-demand eLearning Course helps you, as an Investigator, avoid today's most common inspection findings through practical, memorable application of the Good Clinical Practice (GCP) E6 guideline, and as a result reduce risk and attract more clinical trials to your research site. By highlighting today's most common inspection findings — and providing you with best practices, illustrations and examples for avoiding them through correct application of GCP guidelines — this course will better prepare you for audits/inspections.

Risk-Based Monitoring: The Essentials for CRAs
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Risk-Based Monitoring: The Essentials for CRAs

NEW ACRP's on-demand eLearning Course empowers you, as a Clinical Research Associate (CRA), to successfully prepare for and execute Risk-Based Monitoring plans. This course provides you with a brief history on how Risk-Based Monitoring came about, how it is defined across the world, and most importantly how it will affect your work as a CRA.

Risk-Based Monitoring: The Essentials for CRCs
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Risk-Based Monitoring: The Essentials for CRCs

NEW ACRP's on-demand eLearning Course prepares you, as a Clinical Research Coordinator (CRC), to make the necessary adjustments at your site for execution of Risk-Based Monitoring and equips you to work effectively with Clinical Research Associates (CRAs) carrying out this monitoring approach. This course provides you with a brief history on how Risk-Based Monitoring came about, how it is defined across the world, and most importantly how it will affect your work as a CRC (or research nurse, clinical trial assistant, trial assistant, project assistant).

Risk-Based Monitoring: The Essentials for Investigators
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Risk-Based Monitoring: The Essentials for Investigators

NEW ACRP's on-demand eLearning Course empowers you, as an Investigator, to modify your site quality control plans and to adjust your processes in preparation for executing Risk-Based Monitoring strategies. This course provides you with a brief history on how Risk-Based Monitoring came about, how it is defined across the world, and most importantly how it will affect your work as an Investigator.

Mastering the Event Reporting Cycle: Understanding Your Impact on Patient Safety
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Mastering the Event Reporting Cycle: Understanding Your Impact on Patient Safety

NEW ACRP's on-demand eLearning Course allows you to more efficiently and readily identify and report safety events during the conduct of a clinical trial, regardless of your individual role on the clinical research team. By guiding you through an interactive exploration of the event reporting cycle — from identification to sponsor notification, and from regulatory reporting to Investigator Brochure updates — this course provides you with full comprehension of the roles and responsibilities of site, sponsor and CRO personnel (as defined in the E2a and E6 guidelines) and how your specific role ultimately contributes to patient safety.

Theory to Practice: Operationalize Your Clinical Study Protocol
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Theory to Practice: Operationalize Your Clinical Study Protocol

NEW ACRP's on-demand eLearning Course empowers you to improve and enhance protocol interpretation and conduct, as well as protocol feasibility studies. By guiding you through a mock protocol review, this course ensures you are exposed to statistical considerations for clinical trials (as defined in the E9 Guideline) and that you are able to operationalize your study protocol through comprehension of clinical trial development and design, data analysis, safety and tolerability evaluations, and reporting requirements.

The Drug Development Process: Improving Trial Feasibility and Exploring Your Growth Potential
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The Drug Development Process: Improving Trial Feasibility and Exploring Your Growth Potential

NEW ACRP's on-demand eLearning Course helps you improve your site's feasibility and protocol evaluation practices and prepares you to effectively consider potential avenues for business growth by breaking into additional phases of clinical research. By following a mock drug through a review of the drug development process, this course provides you with a holistic perspective — from the pre-clinical beginning through the four phases of clinical research and beyond, as defined in the E8 guideline — and equips you with easy-to-apply tools for evaluating a site's feasibility to conduct research in each trial phase, as well as protocol feasibility to meet drug development plan goals.

Building Quality Management Systems for Sites and Sponsors: Root Cause and CAPA
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Building Quality Management Systems for Sites and Sponsors: Root Cause and CAPA

NEW The clinical research industry is undergoing a paradigm shift; it’s moving from a focus on detecting and fixing problems to a focus on preventing them, and sponsors and sites are implementing quality management systems to successfully make the switch. You should take this eLearning Course because it will develop or enhance your ability to contribute to the improved quality of your clinical trials by using tools such as ‘Corrective Action Preventive Action (CAPA)’ and ‘Root Cause Analysis (RCA),’ and by applying methodologies and key factors such as documentation best practices and risk management strategies that support and enhance the excellence of a quality management system.

Key Skills for Ensuring Quality Control through Risk-Based Decision Making
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Key Skills for Ensuring Quality Control through Risk-Based Decision Making

NEW Risk-Based Monitoring (RBM) is an approach to quality control conducted by the sponsors of clinical trials that has grown in popularity in recent years, impacting both site and sponsor personnel. Overall trial execution in itself hasn’t been affected by this change. We all have the same end goals in mind: ensuring that trial subjects are safe at all times and that the products that make it to market do so based on decisions that have their origin in accurate and complete data. Quality control is and always has been a key task to meet these goals. A key skill to ensure risk-based strategies and to provide the most secure quality control is the ability to make risk-based decisions. You should take this eLearning Course because it will help you to make the right risk-based decision at the right time, ensuring no harm is done.

Training Packages
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Training Packages

Maximize your training investment with a 20% discount when you "bundle" ACRP eLearning Courses through Training Packages. ACRP is the only organization offering comprehensive training packages on the International Conference on Harmonization (ICH) guidelines critical to the conduct of clinical trials. Training packages are customized for CRAs, CRCs and Investigators to ensure relevancy to your specific role, and are designed to improve your performance in the conduct of clinical trials.

ACRP Certification Exam Preparation
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ACRP Certification Exam Preparation

ACRP's on-demand eLearning Course provides guidance on how to prepare for an ACRP Certification Exam (e.g., CCRA®, CCRC®, and CPI®) to candidates eligible to take the exam. Familiarize yourself with the format of the exam, tackle example questions, and conduct a personal gap analysis to ensure you are fully primed to earn your ACRP Certification.

ACRP Certification Exam Prep Packages
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ACRP Certification Exam Prep Packages

Getting ready to take your Certification Exam? It is recommended that exam candidates begin to prepare three to six months prior to attempting an exam. ACRP offers five options to help you prepare for the exam and earn your Certification in the job-specific function you actually perform, including a variety of Prep Packages.

Resources

  • eLearning FAQs
    Answers to the most common questions about ACRP's eLearning Courses.


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