Courses
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 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.
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.
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 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.
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,…
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.
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.
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.
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,…
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.
