The course provides a thorough Foundation, Advanced and Project Management related concepts focusing clinical trials, drug development, Study design, Project Management, and Monitoring concepts of Clinical Sciences in reference to roles and responsibilities performed by Clinical Research Associate. The concepts include a protocol development, assessment and reporting of adverse events and explains GCP-ICH guidelines along with other necessary regulatory information. The course emphasizes on understanding of the science and the expectations of initiating, conducting, monitoring, and managing clinical trial related work. This training will develop the technical skills and knowledge pertaining to roles and responsibilities of CRA – In House. Students will get exposure to real time practices pertaining to Case Report forms (CRFs), Trial Master File (TMF), Clinical Trial Protocol, Clinical Trial Budget, and Audit. The course curriculum is designed to give an edge to obtain job opportunity in clinical research field.
Our Programs are delivered in 3 Different ways for convenience of student:
Pure Internet Program (PIP)
- A Self-Paced Online Program with Email Support
Blended Internet Program (BIP)
- A Self-Paced Online Program with Email Support Provided (WebEx Online Classes)
Blended Classroom Program (BCP)
- On-Site Faculty based Classes, along with Email Support (On-Site Class)
|Lessons: 41 Lessons||Duration: 08 Weeks / 200 Hours||Language: English|
Clinical Research Associate / Coordinator program is Approved by New Jersey Department of Education and Department of Labor and Workforce, United States.
Recommended:Minimumbachelor's degree in Medicine,Nursing,Pharmacy, Public health Biology, Biochemistry, Biotechnology, Chemistry, Clinical Research, Biomedical engineering, Public health, Pharmacology, or toxicology, Medical Device & Technology, Psychology, Sociology and Healthcare Administration.
The Benefit Student Gains
1) Upgrading the Knowledge required.
2) Better Resume Placement for promising jobs.
3) Low Investment, high learnings
4) Learn from Anywhere, Anytime at your pace.
5) Job and Title Based Tasks as followed and Practiced in industry
6) Applying Concept into Real-time (Policies, governance and tools)
7) Work on Role Based Tasks followed and Practiced in industry
8) Mocks and Narratives for Client Discussions
9) Readiness to work with limited support
Our objective is to help students to meet the following career pathways. Typical Clinical Research Associate (CRA) Job Titles the candidates can apply after this training program are:
Institutional Scholarship / Promotion is available for selected on tuition. We review your education background, certifications, and prior experiences (if applicable), to evaluate your eligibility. Qualified student will be provided with the promo code for scholarship on Tuition.
Please Email your resume to Human Resources email@example.com to check on your eligibility. We will contact you. Qtech's objective is to provide you the right career pathway and advancement required to meet your career goals.
Program is designed by industry experts meeting job and title-based learnings needed for students and young professionals to get into jobs. The training provides in depth knowledge of roles and responsibilities of Clinical Research Associate/ Clinical Research Coordinator. The curriculum includes theoretical and practical aspect of the role and tasks performed on day-to-day basis, along with exposure to various exercises per industry requirements.
3.00 average based on 2 ratings
- Maureen D (Texas)
- Gamal A (New Jersey)
- Sangeetha T (Texas)
3 Executive Drive
Suite 320, Somerset
New Jersey 08873 USA