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Clinical Study Coordinator

also referred to as: Research Coordinator, Site Coordinator, Clinical Coordinator

Content: Historical events that shaped today’s research platform, Protocol and Informed Consent Form (ICF),ICH/GCP and CFR 21,…

Learning: 80-100 hours online and self-paced, 8 Modules, Final Exam

Certificates: GCP, VIARES

Prerequisites: ideally life science education – no work experience required

pay in 12 monthly installments or save with our optional 1-time payment

More than a Course

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.

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 Research Coordinator, also known as Site Coordinator or Study Coordinator.

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

The Training includes access to all Academy Services, and an industry recognized Professional Certification.

  • modules including
    • e-learnings
    • assignments
    • knowledge checks
  • VIARES ACADEMY certificate
  • GCP certification
  • Principle Investigator  Role certificate
  • Set clear goals
  • Get properly trained
  • CV, CV, CV
  • Ace Your Interview
  • Negotiate
  • Weekly new Global Jobs
  • Skip the Application Line
  • Join Career Events

Course Program

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 and two more.

  • •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

Get a PDF of all training details to view more details about each module and view testimonials from past participants:

"The VIARES Clinical Research Program was a fantastic opportunity to gain and update on new knowledge in the field of Clinical Research encompassing Clinical Trials. Overall it was a very good experience with quite intensive learning and an amazing learning and skill development opportunity."
Aniket N VIARES Graduate

Start today

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.

Your expert instructor

Patricia Hollis VIARES Clinical Research Training Course Trainer
Patricia Hollis

Who should attend the Course

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@theviares.com and we will contact you.

Course fees

The fee includes:

  • registration fee
  • all online-training course material, 100% online available in our learning management system
  • module check points (mini-exams during the training to test your knowledge)
  • end-term exam
  • VIARES and GCP certificates upon successful completion of the end-term exam

plus exclusive VIARES benefits:

  • get automatically accepted as Ambassadors and earn cash
  • join career events at no cost
  • free access to our weekly updated global job list
  • apply to exclusive job offers
  • get your personal career coaching
 

Jobs matching this Course

This is a snapshot of 10 latest new entries from our full list of 6,313 Global Clinical Research jobs. Our list is updated and curated for you daily, adding hundreds of new jobs.

Position - click to go to jobCompanyLocationDate CreatedSourceTitle
Position - click to go to jobCompanyLocationDate CreatedSourceTitle

Get a PDF of all training details to view more details about each module and view testimonials from past participants:

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Aniket N
VIARES Graduate
"The VIARES Clinical Research Program was a fantastic opportunity to gain and update on new knowledge in the field of Clinical Research encompassing Clinical Trials. Overall it was a very good experience with quite intensive learning and an amazing learning and skill development opportunity."

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