CRA ACADEMY

CRA Training and more

We help you to improve your employability as clinical research professionals. Our setup enables you to complete your training on your own pace and even next to a full-time job. On successful completion of this program you will have acquired knowledge, skills and competencies to start an entry level CRA or similar roles.

Your training is free and you can start today. If you want to get instructor support from industry experts and industry certification, you can select from one of our affordable upgrades.

Free Training Program

Your training is ready for you today and you have access for three months. Successfully complete eight training modules covering nineteen e-learnings.

  • Background of medicines development
  • Research and discovery stage & product development
  • Clinical development
  • Regulatory submission, Health Technology Assessment, lifecycle management
  • ICH GCP and other applicable regulations
  • The Study Protocol
    • Elements of a Study Protocol according to ICH GCP
    • Trial Design
    • Methodologies
  • Roles and Responsibilities
    • Ethics Committees
    • Sponsor / Monitor
    • Investigator
    • Competent Authority
  • Patient Protection
    • Patient Information
    • Collecting Patient Consent
    • Special Patient Populations
  • Adverse Event Reporting
    • Types of Adverse Events
    • Identifying and Reporting Serious Adverse Events
  • Selecting an Investigational Site
    • Assessing Investigational Sites
    • Training and Upgrading Investigational Sites
  • Initiating Investigational Sites
    • Organizing the Initiation Visit
    • Setting up the required documentation – Essential Documents
  • Effective Monitoring
    • Planning, Conducting, Documenting, and Reporting Monitoring Visits
    • Managing Issues
  • Closing Investigational Sites
    • Organizing the Close-Out Visit
    • Documentation
    • Reporting
  • Managing the Investigational Medicinal Product
    • Definition of investigational medicinal product (IMP) / study drug
    • Provision of the IMP
    • Drug Accountability
    • Randomization, blinding and un-blinding processes
    • Managing Expiry Dates
    • Collecting IMP after Site Close-out
  • Data Collection
    • Clinical Research Form (CRFs)
    • Process of Data Collection
    • Data Collection Systems
  • Data Validation
    • Data validation process
    • Query Process
    • Data Quality Assurance
  • Applicable international and national regulations
  • ICH GCP E6 (R2)
  • FDA Regulation
  • Quality Assurance: Audits and Inspections

Flexible Upgrades

Once you have completed your free training, you can choose from our upgrade options for taking your test and get your personal VIARES Academy Certification. Our three upgrades are flexible and affordable.

You want to take your test and complete the academy on your own? Then this plan is best for you.

The plan includes:

  • 8 knowledge checks
  • VIARES Academy Certification upon successful completion of your tests

You prefer to learn from our expert instructor on top of your self-paced learning experience? Then this plan is right for you to complete the Academy at your own pace and get additional insight from our experts. 

The plan includes:

  • 8 instructor led live webinars, you will get the dates upon signup for the upgrade
  • 15 assignments to apply your learning including feedback from our expert instructors
  • 8 knowledge checks
  • VIARES Academy Certification upon successful completion of your tests

You prefer to learn from our expert instructor on top of your self-paced learning experience? You want to get ACRP certified and differentiate you from other candidates? Then this plan is right for you to complete the CRA Academy at your own pace and get additional insight from our experts. You can start your ACRP membership right after completion of the CRA ACADEMY and get prepared for the ACRP certification.

The plan includes:

  • 8 instructor led live webinars, you will get the dates upon signup for the upgrade
  • 15 assignments to apply your learning including feedback from our expert instructors
  • 8 knowledge checks
  • VIARES Academy Certification upon successful completion of your tests
  • 12 months ACRP Membership upon completion of the VIARES Academy
  • ACRP Certification during your ACRP membership

Academy Dates

Join our webinars with industry expert instructors to foster your module learning and discuss real-life cases with them. If you miss a webinar, you can listen to the recording.

LIVE WEBINARS 

Kick-Off

November 04, 2019

Medicines Development Process, Good Clinical Practice

November 11, 2019

Clinical Trial Design & Roles and Responsibilities

November 14, 2019

Patient Protection & Adverse Events

November 19, 2019

Selecting and Initiating Clinical Trial Sites

November 21, 2019

Monitoring and Closing Clinical Trial Sites

November 25, 2019

Investigational Medicinal Product Management

November 28, 2019

Data Management for Clinical Research Associates

December 02, 2019

Regulatory Environment in the EU and USA

December 05, 2019

​All webinars start 11am EST and are set for 60 minutes.

Should I sign up?

This academy will be of benefit you if you want to drive a career as a clinical research professional. You will get the most out of it, if you have

  • a university degree in life sciences or natural sciences, or
  • first clinical research work experience, or 
  • study site work experience

We are happy to help you make the right decision. Email us at academy@viares.at and we will review with you.

Want to learn more?

Listen to our previous participants!

Listen to our previous participants!

Not yet ready to invest in your career? Sign up to our email list and we’ll keep you updated about our upcoming academy dates!

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CRA Academy

You’re only 1 click away from changing your life. What are you waiting for?

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