Clinical Study Coordinator II

extend your Study Coordinator knowhow: ALCOA-CCEa, Adverse Event, Serious Adverse Events,
ConMeds Log, Screen Visit and Baseline Visits and much more relevant for every Study Coordinator.

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 grow into an intermediate 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:

  • 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 II 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 – VIARES Academy Certificate

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

  • ALCOA-CCEA Principles
  • Source DocumentsTypes
  • Correction Methods
  • Schedule of Events
  • Informed Consent Form (ICF)
  • Informed Consent Process
  • Elements of an ICF
  • Medical History
  • Source Documentation
  • Concomitant Medication (ConMeds
  • Schedule of Events
  • Source Documents
  • Inclusion/Exclusion Criteria
  • Eligibility
  • ConMeds
  • Medical History
  • Source Documentation
  • ConMeds
  • Medical History
  • Adverse Events (AE) and Serious Adverse Events
  • Day 3 procedures
  • New AE/ConMeds
  • Medical History/AE/ConMeds reconciliation
  • Protocol Deviations
  • Day 7 procedures
  • New AE/ConMeds
  • Medical History/AE/ConMeds reconciliation
  • Protocol Deviations
  • Day 14 procedures
  • New AE/ConMeds
  • Medical History/AE/ConMeds reconciliation
  • Protocol Deviations
  • Day 28 procedures
  • New AE/ConMeds
  • Medical History/AE/ConMeds reconciliation
  • Protocol Deviations

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

Joe-Henry

Joe-Henry

It was a great experience to have gone through the VIARIES Clinical Research Talent Program, which was a breath taken opportunity for me as the course gave me the opportunity to broaden my perspective in regards to the dynamics of

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clinical research. The online learning platform was very informative, well organized, and very inspiring for the future Clinical Research professionals. I particularly enjoyed the online webinars and assignments, which made the content understandable. I strongly recommend it to all folks interested in the field of clinical Research. Finally, many thanks to Dietmar Eglhofer and team for ensuring to provide quality t raining.

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Sitakshi

Sitakshi

It was a great opportunity taking part in the VIARES clinical research talent program to build and upgrade my clinical research skills. Since the course offers a nice balance between online webinars, recorded lectures and homework’s which allow us

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to deepen our understanding and apply the concept in real life approach. The program was well organized and excellently structured where the topic was taught by experts in the field. Hence, I am proud to announce that I have successfully passed the final exam and would recommend to those, who is seeking a rewarding carrier in clinical research. I personally thank to Mr. Dietmar Eglhofer and team for running this amazing platform and giving us the opportunity to be a part of VIARES Academy.

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Clinical Study Coordinator II
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£ 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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