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.
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.
Becoming a clinical study coordinator can be a rewarding career path for a number of reasons. Here are a few potential reasons why you may want to consider this profession:
Of course, becoming a study coordinator also requires hard work, attention to detail, and a commitment to accuracy and compliance. But if you are passionate about medical research and helping others, it could be a rewarding and fulfilling career choice.
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 start at an entry 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!
Certificates:
Life-time payment plan includes:
Monthly payment plan includes:
The responsibilities of a clinical study coordinator can vary depending on the specific study or trial they are working on, as well as the organization or institution they are employed by. However, some typical responsibilities of a clinical study coordinator may include:
Overall, the role of a clinical study coordinator is critical to the success of any medical research study or clinical trial. By ensuring that the study is conducted ethically and according to regulatory requirements, and that data is collected accurately and securely, study coordinators help to advance our understanding of disease and improve patient care
The specific educational and professional background required to become a clinical study coordinator can vary depending on the employer and the specific job requirements. However, most employers prefer or require candidates to have a bachelor’s degree in a related field such as nursing, biology, life sciences, or a health-related field. Some employers may also prefer or require candidates to have a graduate degree such as a master’s degree in a related field.
In addition to education, employers typically look for candidates with relevant experience in the field of clinical research or healthcare. Clinical experience, such as experience as a nurse or medical assistant, may also be valuable.
Other important qualifications for a clinical study coordinator may include:
Overall, a background in a related field, such as healthcare or life sciences, combined with relevant experience and key qualifications can prepare you to become a successful clinical study coordinator.
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.
Getting a clinical study coordinator certification can be a valuable step in advancing your career and demonstrating your expertise in the field. Here are a few potential reasons why you may want to consider pursuing certification:
Enhancing your credentials: A clinical study coordinator certification can demonstrate to employers, colleagues, and patients that you have met certain professional standards and have a certain level of expertise in your field. This can be particularly important in a field as highly regulated as clinical research.
Improving your job prospects: Having a certification can make you a more competitive job candidate and can help you stand out in a crowded job market. Some employers may even require or prefer that their clinical study coordinators have certification.
Continuing education and professional development: Many certification programs require ongoing education and training to maintain the certification. This can be a way to stay up-to-date with the latest developments in the field and to continue developing your skills and knowledge.
Overall, getting a clinical study coordinator certification can be a valuable investment in your career and can help you demonstrate your commitment to excellence in the field of clinical research.
This is a snapshot of the latest new entries from our full list of global clinical research jobs. Our list is updated and curated for you daily, adding hundreds of new jobs. Get full access with a VIARES account.
| Position – click to go to job | Company | Location | Date Created | Source | Title | Id (key) |
|---|---|---|---|---|---|---|
| Position – click to go to job | Company | Location | Date Created | Source | Title | Id (key) |
I really enjoyed the VIARES clinical talent program. I’ve learned a lot about the design, regulation and management of clinical trials. This course offers a nice balance between recorded lectures, live webinars and homework that allows you
[expand]
to deepen your understanding and apply some of the concepts taught.
[/expand]
The VIARES Talent Program opened the doors to the fascinating world of clinical trials and covered all aspects of the field. The course was very well-organized and detailed. The instructors were knowledgeable, enthusiastic, and provided real-world
[expand]
insights. The assignments really helped to internalize all we had learned throughout the course.
[/expand]
reviews curated by judge.me
BESTSELLER
Grow your career into a Project Management with you new skills on Project Management Basics, Stakeholder Management, Project Planning, Project Risk Management, Clinical Risk Management,...
Get to know the basics of clinical research. 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 in clinical research.
NEW COURSE
£ 14.90 / month for 12 months/m £ 149.90
Start your clinical research career and unterstand the role and responsibilities of a Trial Master File Specialist during Clinical Trials. Take on roles responsible for managing the Trial Master File, which is the collection of all essential documents related to a clinical trial.
£ 149.90
£ 14.90 / month for 12 monthsPay monthly
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 © 2022. All rights reserved.
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.
