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.
With the All-In-One package you get all training courses. Experience the full strength of the VIARES and get the utmost competency development.
You will get your personal certificates as you complete the training courses.
But that is not all. You get professional career support from VIARES.
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.
I’m glad to share that I was part of VIARES Clinical Research Talent Program. VIARES CRTP is well balanced which gives you new skills and opportunity to be part of the huge CRA’s family. The program contains well-organized micro – courses,
[expand]
webinars which are prepared by true professionals. Thank you for that scientific journey.
[/expand]
reviews curated by judge.me

BESTSELLER
€ 674,90 Original price was: € 674,90.€ 269,90Current price is: € 269,90.
€ 674,90 Original price was: € 674,90.€ 269,90Current price is: € 269,90.
Get new job posts and all the news about our VIARES clinical research courses in your inbox!
Our support and sales team is available 24 /7 to answer your queries.
Clinical Research Training courses
all prices incl. VAT
Copyright © 2023. All rights reserved.
certified Lead Auditor for ISO 9001:2015
Kamila Novak, MSc, has been involved in clinical research since 1995, having worked in various positions in pharma and CROs. Since 2010, she has been working as an independent consultant in medical writing, auditing, training, project and risk management. She delivered dozens of courses in areas related to clinical research and project management. In August 2019, Kamila became a certified Lead Auditor for ISO 9001:2015. Kamila is a Core Team Member in the DIA GCP & QA, Clinical Research, and Project Management Communities.
Data Scientist at Whythawk
Gavin Chait is a Data Scientist at Whythawk, which specializes in integrated open data consulting, and training for open knowledge, freedom of information, and economic development projects. He spent more than a decade in economic and development initiatives in South Africa. He was a commercial director at the Open Knowledge Foundation, and led the implementation of numerous open data projects around the world. Gavin has twenty years of experience in teaching at all academic levels, and is a passionate advocate for knowledge development through open access to data and freedom of information.
in the industry for 21 years
Patricia has been in the clinical research industry for over 20 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.
18 Years experience
Bartek has 18 years experience in clinical research business, mostly spent at largest global Contract Research Organizations. At Quintiles he was responsible for pioneer development of clinical start-up and regional contract departments. He served as executive member of clinical start-up leadership team at INC Research, acting as global head of site contract division. His most recent experience includes support for pharmaceutical organizations in various project specific roles. Bartek enables biopharma to get their sites up and running faster. He is author of several training programs about site contract related matters and successfully delivered to hundreds of individuals worldwide.