TOP SKILL 2024
Are you ready to master the latest changes in the pharmaceutical industry? Our comprehensive online course is designed to guide you seamlessly through the transition from ICH-GCP E6(R2) to (R3). Whether you’re a professional in the pharmaceutical sector, a clinical researcher, or a regulatory affairs expert, this course is tailored to elevate your understanding and application of the new ICH guidelines.
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.
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,…
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.
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.
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,…
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.
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.
INDUSTRY SPONSORED PROGRAMS
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.
We support your application process
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.
