Successfully complete the 8 competency modules below to obtain your VIARES Academy 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.
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.
There are several reasons why you might consider becoming an advanced clinical study coordinator:
Overall, becoming an advanced clinical study coordinator can be a rewarding and fulfilling career path with opportunities for growth, job security, and competitive compensation.
The responsibilities of an advanced clinical study coordinator can vary depending on the organization and the specific clinical trial or study they are working on. However, here are some typical responsibilities you might expect in this role:
Overall, the role of an advanced clinical study coordinator is to manage and coordinate all aspects of clinical studies, from study planning and design to study closeout. Effective coordination and communication with all stakeholders involved in the study, including study participants, principal investigators, and regulatory agencies, is essential to ensure the success of the study.
To become an advanced clinical study coordinator, it’s typically necessary to have a background in a health-related field, such as nursing, pharmacy, or healthcare administration. Here are some of the qualifications and skills that are often required or preferred for this role:
Overall, a combination of education, experience, and specialized skills is required to become an advanced clinical study coordinator. However, there are many different pathways to this career, and some employers may have specific requirements or preferences depending on the type of studies they are conducting.
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 certification as an advanced clinical study coordinator can provide several benefits, both for your career and for the clinical research industry as a whole. Here are some reasons why you might want to consider getting certified:
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) |
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!
Certificates:
Life-time payment plan includes:
Monthly payment plan includes:
It was a pleasure to take part in the VIARES Clinical Research Talent Program. I gained so much knowledge and understanding of clinical research. I would recommend it to anyone who is interested in the field of clinical trials.Many thanks to Dietmar
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Eglhofer, the whole team and all amazing tutors for providing this informative and very-well organized program
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VIARES provided me with the formal training and skills that would allow me to achieve my career and personal goals. A chance to complete this course afforded me the opportunity to experience the clinical trial training from different experienced
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professionals, whilst providing me with exposure to the international arena of clinical research management and the global concerns while interacting with the multi-national specialists and students. I developed skills in report writing, clinical trial design, and data management among others. I would recommend the VIARES ACADEMY for anyone eager to set strong foundations in clinical research whilst remaining all rounded.
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BESTSELLER
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.
TOP GRADUATE PROGRAM
£ 14.90 / month for 12 months/m £ 149.90
The Clinical Trials MasterClass is specifically designed for graduates with a bachelor’s degree or higher and little or no active work experience. Even without any related background, this MasterClass will get you ready for entry level jobs in the clinical research industry.
CUSTOMER TOP CHOICE
£ 14.90 / month for 12 months/m £ 149.90
On successful completion of this course, you will be certified and will have acquired knowledge, skills and competencies to start at an entry level role as Clinical Research Associate, In-House Clinical Research Associate or similar.
£ 149.90
£ 14.90 / month for 12 monthsPay monthly
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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.
