Clinical Study Coordinator I

also referred to as: Research Coordinator, Site Coordinator, Clinical Coordinator
Historical events that shaped today’s research platform, Protocol and Informed Consent Form (ICF),ICH/GCP and CFR 21,…

Description

A Flexible Online Setup

Our setup enables you to complete this program either next to a full-time job or in a focused effort. 100% of the program is online and most of the training courses can be completed at any time.

You can start the training right away and complete it at your own pace. This training contains 100 hours of online material.
You do not need to wait for a kick-off date, you can start your training anytime  – as early as today if you wish.

Get Certified & Job Ready

On successful completion of this program, you will be certified and will have acquired knowledge, skills and competencies to start at an entry level role as Clinical Study Coordinator, Clinical Research Coordinator, or similar.

The VIARES Clinical Study Coordinator program is more than just a training. It’s a life-changer!

Certificate:

  • GCP
  • VIARES
 

The fee includes:

  • registration fee
  • all online-training course material
  • one year online access to our learning management system
  • mini-exams during the training to test your knowledge
  • VIARES exam of 100 question
  • personalized certificate upon completion
 

plus exclusive VIARES benefits:

  • join career events at no cost
  • free access to our weekly updated global job list
  • apply to exclusive job offers

Course Content

The Clinical Study Coordinator training consists of eight consecutive modules. You will complete each module by:

  • taking your e-learning
  • submitting your assignment work
  • completing your module test
  • taking the final exam

8 Modules – 100 Learning Hours – 3 Certificates.

Successfully complete the 8 competency modules below to obtain your VIARES Academy Certificate.

  • Historical events that shaped today’s research platform.
    • Nuremberg Code (1947)
    • Declaration of Helsinki (1964)
    • Belmont Report Principles (1979)
    • National Research Act (1974)
    • International Standard Organization 14155
  • A global response to unethical research
  • International Council of Harmonisation and Good Clinical Practice Guidelines (ICH/GCP)
  • 14 principles of GCP
  • Food and Drug Administration (FDA)
  • Clinical Research Process
  • Study Designs in Clinical Trials
    • Randomization
    • Non-Randomization
  • Phases of clinical research
    • Pre-Clinical
    • Phases I-IV
  • Understand Clinical Research organizational char
    • Clinical Site Organizations
    • Site Management Organizations
    • Vendors
    • Sites
    • Pharmaceuticals/Biopharma
    • Institutional Review Board/IEC
  • Investigators
  • Supplemental research staff
  • Documentation requirements for assigned task
  • CRCs responsibility for managing site staff training and delegation log
  • Delegation Log
  • Clinical Research Protocol
  • Informed Consent Form (ICF)
  • Source Documents
  • Medical Records
  • Standard of Operations
  • Adverse Events
  • Serious Adverse Events
  • Concomitant Medication (ConMed)
  • Medical History-out
  • Monitor Role
  • Visits
    • Selection
    • Initiation
    • Interim
    • Close Out
    • Booster
  • Communication
  • Query Resolution
  • Identifying and resolving site issues

Requirements

This program will be of benefit to anyone with a bachelor degree in life science degree and/or first relevant work experience, ideally in clinical research, pharma or related areas, e.g. working with patients, medical products or services, medical technology, laboratories or similar.

If you are not sure if this is the right training for you, we are happy to help you make the right decision. Email us at academy@viares.com and we will contact you.

Your expert instructors

Hear from our graduates

Suchi

Suchi

I found the VIARES Clinical Research Academy course very informative, well explained and interesting. I come from a completely non-Clinical Research background and found this course quite easy to follow. The content is very apt and to the point. I have

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a strong belief that with this course, I have developed a strong foundation into concepts around Clinical Research, which will pave a long way for my career into the future.

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Matthew

Matthew

As someone who has no monitoring experience, the CRA Academy made it easy for me to understand how the Clinical Research field works. The instructors are easy to understand and they accommodate all queries that we have.

Customer Reviews

Based on 2 reviews
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O
Olga Nonzwakazi Nzamela
5*

Very informative

A
Adedamola Ellis
Class was ok

I loved the class but can you help in actually getting a job. Since most of the companies are not hiring me.

reviews curated by judge.me

 
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Clinical Study Coordinator I
This Course includes

£ 159.90

£ 19.90 / month for 12 monthsPay monthly

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      PATRICIA HOLLIS

      in the industry for 21 years

      Patricia has been in the clinical research industry for 21 years. She began her career as a clinical research coordinator at the Medical College of Virginia where she coordinated pharmaceutical and PI initiated trials. She has been a Clinical Research Associate for 16 years and has had the opportunity to serve as a Lead CRA, Clinical Trial Manager, Auditor, Mentor, and Clinical Research Instructor. She has worked in all phases of research and is experienced in numerous therapeutic areas, including Oncology, Endocrinology, CNS, Immunology, Cardiology, Nephrology and Device. Currently, she is a contract CRA through her company, The Hollis Group, LLC, which she owns with her husband and serves as a consultant at local research sites. Patricia completed a Bachelor of Science degree at Virginia Commonwealth University, MBA at Texas Woman’s University and has had specialized oncology training from the Oncology of Nursing Society.

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