ALL COURSES FOR THE PRICE OF 2!
Transform your clinical research career with our comprehensive training bundle! By enrolling in all courses, you’ll gain expertise across trial documentation, monitoring trials, project and site management, regulatory compliance, oncology research, remote monitoring and all you need for your clinical research career.





With the All-In-One package you get all 14 training courses. Experience the full strength of the VIARES certifications and get the utmost competency development.
Start your journey as a Clinical Trials Assistant! This course gives you foundational knowledge in clinical research, trial documentation, and data management. Learn essential skills to support clinical trials efficiently, making a real impact in the field of medical research—enroll now and start building your expertise!
Jumpstart your career in clinical research! Gain essential TMF skills to manage trial documentation, ensure compliance, and meet regulatory standards. Become the specialist top organizations need—enroll now and elevate your expertise in clinical trial management.
Navigate ICH-GCP E6(R3) standards with confidence! This course provides comprehensive training on ethical guidelines, regulatory compliance, and trial management. Gain the expertise needed to ensure high standards in clinical trials worldwide—start enhancing your clinical research knowledge today!
Become a Study Start-Up Specialist and master the processes that bring clinical trials to life. Learn key regulatory requirements, submission strategies, and project initiation skills to ensure compliance and efficient trial launches. Start building your expertise in clinical research today!
Drive clinical trial success as a Clinical Operations Specialist! This course gives you expertise in trial design, regulatory compliance, and site management to ensure seamless operations. Build a career in clinical research with skills that global organizations value—start now!
Accelerate your career as a Clinical Research Project Specialist! This course equips you with skills in project design, compliance, and stakeholder communication. Learn to manage clinical trials effectively, ensuring successful project outcomes. Start making an impact in clinical research now!
Launch your career as a Clinical Study Coordinator! This course provides essential skills in study design, site management, and regulatory compliance, preparing you for a pivotal role in clinical trials. Gain practical knowledge to support groundbreaking medical research—your journey starts here.
Advance your skills as a Clinical Study Coordinator! This course covers ALCOA-CCEa principles, patient consent management, and precise data handling. Gain critical expertise in eligibility assessment, adverse event management, and documentation accuracy—step up in clinical research now!
Advance as a Clinical Study Coordinator! Gain expertise in IRB management, regulatory compliance, and precise trial documentation. Build specialized skills in FDA forms, protocol deviations, and investigational product handling—excel in complex clinical research responsibilities today
Step into the role of a Clinical Research Associate! This course covers clinical trial management, regulatory compliance, and data quality. Master the skills to monitor trial sites, ensure patient safety, and support groundbreaking research—your career in clinical research starts here.
Master remote and centralized monitoring for clinical trials! This course equips you with regulatory knowledge, risk-based monitoring skills, and daily workflows for remote oversight. Start shaping your expertise in modern monitoring methods to excel in clinical research—enroll today!
Specialize as an Oncology CRA! This course provides key skills in oncology trial monitoring, patient safety, and compliance with industry standards. Gain expertise in managing complex oncology trials and become a valuable asset in clinical research—start advancing your career in oncology today!
Grow your career in Clinical Project Management with our Academy! Build your new skills around Project Management , Stakeholder Management, Risk Management, Budgeting and many other job-relevant skills, to step our of your current role and become a Clinical Project Manager.
Are you dreaming of a career in clinical research but struggling to land your dream job? If so, you’re not alone. Many aspiring professionals find the job search process challenging and overwhelming. That’s why we created the Clinical Research Career Accelerator.
Explore the full curriculum in pdf and receive email reminders when enrollment closes:
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Online Self-paced
learn at your own schedule and pace
6 small monthly payments
one discounted payment
one payment – access forever
We pride ourselves on high-quality programs. That’s why we offer a 5-day no-questions-asked 100% money-back guarantee. If for any reason you are unhappy, you will get a full refund.
Your membership to VIARES includes everything you need to excel in your clinical research career.
Connect with peers worldwide to share insights, best practices, and engage in thought-provoking discussions.
Redefine your career trajectory and fast-track your personal growth with powerful career mapping and feedback tools.
Develop the latest and most in-demand clinical research skills with 100% online and globally recognized courses.
VIARES is known by the world’s leading organizations for for clinical reasearch providing you with the best training for your future dream job!
With VIARES you also get support with finding your clinical research dream job.
VIARES’ digital certificates are a proven way to showcase that you mastered a new skill and upgrade your resume to land your next dream job.
Becoming a Trial Master File (TMF) Specialist can be a rewarding career path for individuals who have a strong attention to detail and organizational skills, as well as an interest in clinical research. Here are some reasons why you may want to consider becoming a TMF Specialist:
In summary, becoming a TMF Specialist can offer a challenging and rewarding career path for individuals who are interested in clinical research and have strong organizational skills. The role offers job security, growth opportunities, and the ability to make a meaningful contribution to medical research.
The responsibilities of a Trial Master File (TMF) Specialist can vary depending on the organization they work for and the specific clinical trials they are involved in. However, here are some typical responsibilities that a TMF Specialist may have:
Overall, the TMF Specialist plays a critical role in ensuring that clinical trials are conducted in accordance with regulatory requirements and industry best practices, by managing and maintaining the essential documents related to the trial.
Upon enrollment you will receive your first certification “Confirmation of Enrollment”. After successful completion of the course and your exam, you get your personal “Course Certificate” including:
We also show you how to best share your certificate on LinkedIn and other social media platforms.
There are several reasons why you might consider getting a CRA certification:
Demonstrated knowledge and commitment: Obtaining a CRA certification demonstrates to employers and colleagues that you have a strong understanding of clinical research processes, regulations, and best practices. It shows your commitment to your career in clinical research and can set you apart from other candidates when applying for jobs.
Increased job opportunities: Many employers prefer or require candidates with CRA certifications for their open positions. Having a certification can make you a more competitive candidate and increase your job opportunities.
Career advancement: A CRA certification can help you advance in your career by opening up opportunities for promotion, leadership roles, and increased pay.
Continuing education: Many employers require ongoing education and professional development, which can help you stay up-to-date with the latest developments in the field.
Overall, obtaining a CRA certification can help you stand out in a competitive job market, demonstrate your knowledge and commitment to your career, and open up opportunities for career advancement and professional development.
No, you can proceed with the course in your own pace. But please keep in mind, that you might have to purchase a course extension in order to continue learning (check the pricing table above).
To become a CRA, you will typically need a bachelor’s degree in a life science or healthcare-related field, such as biology, chemistry, nursing, or pharmacy. However, some employers may accept degrees in other fields if you have relevant work experience.
In addition to a degree, it is beneficial to have experience working in the healthcare or research industry. This can include positions such as a research assistant, laboratory technician, or nurse. Other skills for a CRA include attention to detail, strong organizational and communication skills, the ability to work independently and as part of a team, and problem-solving abilities. Proficiency in Microsoft Office and other relevant software is also important.
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.
VIARES ACADEMY ALL-In-One
| 5 star | 92 | 92% |
| 4 star | 5 | 5% |
| 3 star | 3 | 3% |
| 2 star | 0% | |
| 1 star | 0 | 0% |
Just finished the VIARES CRA Academy and I’m blown away. Clear, practical, straight-to-the-point lessons that actually prepare you for the real job. Passed the exam first try. Best investment I’ve made in my career. Highly recommend!
Thank you VIARES
Really good work and presentations. I wish live also be a part of it. Otherwise the course is excellent
VIARES ACADEMY ALL-In-One Accelerator
Clinical Research Associate Accelerator
Clinical Research Associate
Clinical Study Coordinator II
VIARES Micro Certificate DOUBLE-BLIND STUDY
Cliniical Research associate Tutorials were very clear and tutors very friendly. Queries were responded to very promptly.
VIARES Micro Certificate PHASES OF CLINICAL TRIALS