There are several potential reasons why you might consider becoming a clinical research professional, including:
Overall, becoming a clinical research professional can be a fulfilling and rewarding career path for those who are interested in contributing to medical research and improving patient outcomes.
To become a clinical research professional, there are several educational and experiential backgrounds that can be helpful, including:
Overall, a combination of education and experience can be helpful for those seeking a career in clinical research. It’s important to stay up-to-date with the latest industry trends and regulations, and to continually seek out opportunities to develop your knowledge and skills in this rapidly-evolving field.
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.
Obtaining a Clinical Research certification can provide several potential benefits, including:
Overall, obtaining a Clinical Research certification can be a worthwhile investment for those who are committed to their career in clinical research and interested in advancing their knowledge and skills.
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 400 hours of online material and you can complete it at your own pace.
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.
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 Clinical Research Starter Package consists of 3 training courses. Successfully complete the courses to obtain three certificates.
After successful completion of all modules, you will be graduating the VIARES program and obtain your certificate.
The VIARES Certification is an online exam covering 50+ questions from the VIARES training course. You need to complete the exam within 60 minutes and achieve at least 80% of all points to be graded positive. You have two attempts, of which the attempt with the higher score is applied for your certification.
After successful completion of the exam, you will be graduating the VIARES program and obtain your certificate.
The VIARES Certification is an online exam covering 100 questions from the VIARES training course. You need to complete the exam within 90 minutes and achieve at least 80% of all points to be graded positive. You have two attempts, of which the attempt with the higher score is applied for your certification.
After successful completion of the exam, you will be graduating the VIARES program and obtain your certificate.
VIARES has revolutionized trainings for Clinical Research Associates. Besides being standardized with industry focused content, the training is well structured and very detailed. The delivery and assessment of content is superb. Coming from Africa
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and a top class training I received at the Academy, I have what it takes to support both operations in the Pharma industry as well as CROs.
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I have successfully completed the VIARES Clinical Research Talent Program, allowing me to expand my clinical research skills. The program has informative micro-courses and webinars which are organized. This program provided me with deep
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insights into clinical research. I highly recommend it to anyone interested in the field of Clinical Research.
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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.
