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Our most comprehensive package includes everything you need to succeed in your fast growing clinical research career. With access to clinical research online courses, MasterClass, and 2 individual career coaching sessions, you'll be fully equipped to take your career to the next level.
Get the VIP package to experience the full power of VIARES, and get ready to excel in your career!
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Our All-In-One package gives you full access to all of our online clinical research courses at a reduced price. With VIARES Clinical Research Training, you'll gain the skills and knowledge you need to succeed. Plus, you'll receive exclusive advice on advancing your career. Select the All-In-One package to unlock your full potential in clinical research!
CUSTOMER TOP CHOICE
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.
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,...
Step up and learn to monitor an oncology study. Add your new competencies in Cancer Treatments, Tumor Staging and Tumor Grading, Oncology Study Design, Clinical Assessments, Lines of Therapies, Oncology Subjects and Enrollment Process, RECIST,...
TOP GRADUATE PROGRAM
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.
The role of a clinical study coordinator is critical to the success of any medical research study or clinical trial. 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 or similar.
NEW COURSE
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.
Get ready for the future of monitoring! Get introduced to monitoring concepts, on-site, remote, and statistical monitoring, Regulatory guidance to remote and statistical monitoring, Monitoring concepts in the framework of risk-based monitoring,...
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.
Start as a specialist in study start up and build your competencies in core submission documents, country level documents for submission, VHP process and timeliness, EudraCT, IP release document requirements,…
Master the world of clinical data with your new skills on Data as a Science, research and experiments with data, probability, randomness and the risk of de-anonymization, sampling, data distribution, and secure data custody,...
Become a Clinical Operations Specialist and contribute to the clinical research team by planning, managing, and executing clinical studies. Learn about Good Clinical Practice, Regulatory Environment in the EU and USA, Clinical Trial Design,...
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.
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.
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Clinical Research Training courses
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