Qtech Solutions Inc.
3 Executive Drive, Suite 320
Somerset, New Jersey USA 08873
Phone : 732-770-4100 Fax: 888-532-0210
Email : firstname.lastname@example.org
Qtech-Sol Training division doing business as Qtech-Sol Professional Development Center (QPDC) is a Private Vocational School and its Clinical Science programs are approved by New Jersey State - Department of Education and New Jersey Department of Labor and Workforce Development. We primarily engage in offering an array of short duration certificate courses for corporate, professionals and students. Our CRA Package program offered, allows you to focus on securing a career advancement job.
CRA Certification and Job Oriented Program (CRAT)
Clinical Research Associate (CRAT) - Certification program - 45 Days
Advanced Clinical Research Associate (ACRA) - 30 Days (Bonus)
Clinical Research Project Management (AACR) - 30 Days (Bonus)
Post Training Assistance (Resume Prep, Narratives and Mock Session) - 15 Days
This program allows you to better place your profile with clients for possible jobs. The job market requires experience and understanding of Clinical Research Operations and the Job tasks performed. Qtech-Sol package program, will provide the required experience to jump-start.
This Training Program as Internship provides students hands-on about the various tasks and duties performed by Clinical Research Associate at Pharmaceutical, Hospital, and Research Organizations towards conduction of Clinical Trials and project management tasks. This Training program is Unpaid Internship and is conducted for 12 Weeks to Fresh and Alumni Students. Selection of Student is based on education background and GPA, subject to Interview performance. Student will participate into this program remotely. Students attending the Training program must plan to spend minimum 4 hours/ day to submit the deliverable per schedule. The lessons will educate the student on the CRA task to perform, client settings followed in Industry, team-work and submit timely the allocated deliverable tasks as part of this learning. During this Training Program, the candidate will have access to Qtech Proprietary forms, data and related presentations. The Student will be exposed to various CRA Job related hypothetical tasks to gain required experience. The tasks are evaluated and feedback is provided via email. Candidates who have successfully completed this program, will be provided a certificate of completion. The student will take a final certificate exam at the end of this training program.Candidate who cannot participate on-site, can participate from their home as virtual-Internship.
Learning’s Gained during this Training Program
Drug Discovery and Research Process
Introduction to Clinical Trials
Role of Clinical Research Associate
Phase I Clinical Trials
Phase II Clinical Trials
Phase III Clinical Trials
Phase IV Clinical Trials
Good Clinical Practice and ICH Guidelines
Institutional Review Board (IRB)
Overview of Clinical Protocol
Clinical Protocol Design and Development
Case Report Form (CRF) Design and Data Capture
Clinical Trial Budget
Conducting Multinational Clinical Trials
Communication with Cross Functional Team
Clinical Research Associate In House Responsibilities
Selection of Investigator
Vendor Selection and Management
Informed Consent Preparation
Roles and Responsibilities of Investigator
Investigator Meetings and Timelines
Selection of Investigator Site
In-House Monitoring and Reporting
Trial Master File (TMF)
Introduction to Adverse Events (AE) Reporting and Classification
Preparation for Internal Audit
: Biology, Biochemistry, Chemistry, Clinical Research, Medicine, Nursing, Pharmacy, Public health, Pharmacology, or toxicology, Microbiology, Psychology and Sociology.