Advanced clinical research

Learn to conduct clinical research, collaborate with clinical scientists, and enhance your skills in patient-oriented research. This course provides training for students to learn how the Clinical Trial Management process works, developing complete regulatory activities involved in creating documents and in planning, organizing, monitoring, recording, analysis, and reporting of clinical trials. The program provides additional opportunities to learn about recent advancements as well as specializations in risk-based monitoring concepts. In This Course Study Startup: Understand the phases of the Clinical Trial, ICH-GCP guidelines, study feasibility, and site selection. Study Conduct: Learn about site monitoring visits, which include remote and central risk-based monitoring. Study Closeout: Learn about site close-out visits including both on-site and remote activities. The Sollers Advantage Work on real-time case scenarios, clinical tasks, and other site management activities taught by industry experts. Understand and implement site selection, site initiation, site monitoring, and various other site activities. Students will assign sites, site staff, IRB, and labs to the pre-designed studies in the CTMS as a CRA. Students work on various documents related to site visits as per the regulatory bodies' requirements. Students will work on the site binder and trial binder in the e TMF system. Students will be working with documentation related to local and central IRB (regulatory board). Course Duration 15 weeks (20+ hours each week) 3 Sessions /week Engagement 150 hours Financial Options Sollers has devised viable financial options for you to ensure tuition does not get in the way of your education. Now, you can focus your attention where it needs to be – in the classroom! After the completion of the program, we assist our students with interview coaching, resume building sessions, conduct mock interviews, job readiness training, and make them competent to venture into the corporate world. We provide exclusive one-on-one sessions with our industry-based career advisors who provide guidance right from resume feedback, assisting with interview Q&As, and helping with job preparations. Minimum Requirements Graduates from science, nursing, pharmacy, medical, dental, and computer backgrounds can take this program. Basic knowledge to work with computers, quick learning aptitude to get trained in newer software application tools, company SOP, medical terminology, clinical SAS, and willingness to travel. Understanding of ICH/GCP clinical trial paradigm, roles and responsibilities of various functionaries of the clinical trial process. Detailed training of Clinical Trial Manager, Monitor, Coordinator, and Data Analyst functions. Be proficient to work on EDC based risk-based monitoring along with user-friendly knowledge of relevant tools like CTMS, e TMF, and Clinical SAS. Clinical research has proven to be exceedingly more necessary by health organizations and pharmaceutical companies in today’s modern age. #J-18808-Ljbffr