As our VIP you get the unique package that consists of all training courses and our MasterClass:
But that is not all. You get personal and exclusive career support from our talent team:
You will get your personal certificates as you complete the training courses.
A Growing Industry
First, the clinical research industry is growing every year by 6-8%. In parallel, the global talent pool grows by about 4-5%, which provides great career opportunities.
If you have the required degree and work experience, it’s your turn to become one of these knowledgeable experts!
Jobs That Pay Well
The number of job opportunities is currently growing. As an example salaries for CRA start at around €35.000 in Europe and $75.000 in the USA and go way above $100.000 per year.
Next to these starting salaries, it is possible to take fast career pathways and gain more responsibilities rapidly. Promotions often come within 2-3 years into professional levels, taking salaries up to about €45.000 in Europe and $100.000+ in the USA.
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 boost your clinical research career.
The training includes access to all academy services, and an industry recognized professional certification.
You can start the training right away and complete it within the given timelines at your own pace. This training contains over 900 hours of online material and you have 12 months to complete it.
You do not need to wait for a kick-off date, you can start your training anytime – as early as today if you wish.
Requirements:
This program will be of benefit to anyone with a 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.
Certificates:
Life-time payment plan includes:
Monthly payment plan includes:
The VIARES CTA Academy is a great resource for those interested in entering the field of clinical research. It provides you with valuable knowledge on multiple topics such as data management, key roles in clinical research, the drug development
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process, and important documentation. After my completion of the VIARES CTA academy, I am confident in my knowledge of the clinical process.
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I recently completed the VIARES Clinical Research Associate (CRA) training course and passed both VIARES and ACRP-ELKA certificate. I found the course is informative, covers a wide range of important topics, from drug development, CRA roles,
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study visits and close-out, and data management. Thank you for the opportunity to learn and looking forward to embarking on this clinical research journey.
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reviews curated by judge.me
BESTSELLER
Start your clinical research career as Clinical Research Project Specialist. Learn the basics on clinical research, regulations and new skills in project management , stakeholder management, project planning and more to support a Clinical Project Manager.
Start your clinical research career as Clinical Trials Assistant. Get certified and acquired knowledge, skills and competencies to start at an exiting clinical research career as Clinical Trials Assistant or similar.
Deepen your know-how as a Clinical Study Coordinator and get upskilled on key areas like ALCOA-CCEa, Adverse Event, Serious Adverse Events, ConMeds Log, Screen Visit and Baseline Visits and more.
£ 399.90
£ 39.90 / month for 12 monthsPay monthly
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Clinical Research Training courses
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Trained in 6 continents
Eric brings with him 20 years of experience training and meeting management and has worked in clinical research for almost 25 years. The global reach of this experience (Eric has trained in six continents) makes him the partner of choice to work with. Eric combines soft skills with personal responsibility in every training.
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.
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.
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.
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.
