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TRANSITION PROGRAM
€ 39,90 / month for 12 months/m € 249,90Applicants with a life-science degree and work experience outside of clinical research only have less than 20% chance to get to an interview for a clinical research job. The Cross Over Program Clinical Research Associate (xCRA) will help you to cross the path from your current job into the clinical research industry.
TRANSITION PROGRAM
€ 29,90 / month for 12 months/m € 199,90The Cross Over Program Clinical Research Assistant (xCRS) will help you to cross the path from your current job into the clinical research industry. This program is designed for anyone without a life-science degree. First work experience is helpful, but not required.
CUSTOMER TOP CHOICE
€ 24,90 / month for 12 months/m € 149,90On 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,...
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
€ 24,90 / month for 12 months/m € 149,90Start 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.
Deepen your know-how as a Clinical Study Coordinator and get upskilled on key areas like Institutional Review Board (IRB), Facilities and Delegation, Inform Consent Log, Subject Logs, Identification Log, Enrollment Log, Form FDA 1572, Form FDA 3455, Protocol Deviations, CAPA, Investigator's Brochure 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.
IQVIA is looking for innovative clinical research professionals just like you to join their Clinical Operations teams across the following European countries: Austria, Belgium, Czech Republic, Hungary, Netherlands, France, Germany, Italy, Poland, Spain, UK
Our academy is your entry ticket and it is completely free of charge for you.
Unlike other pure training companies, VIARES is a Clinical Research Talent Organization. For you this means, we not only provide you with industry relevant top role training, but we also support you in applying for jobs. We help you improve your employability in the fast-growing clinical research industry.
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Clinical Research Training courses
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