New Jersey 732.770.4100
Clinical Research Associate / Coordinator
||Recommended: minimum a Bachelor degree in biochemistry, biomedical engineering, biotechnology,
chemistry, clinical data management, medicine, pharmaceutical engineering, industrial pharmacy,
industrial chemistry, public health, pharmacy, pharmaceutical business, pharmacology, or toxicology.
||The course provides a thorough foundation in clinical trial science, the drug development process,
and clinical trial design methodology. It includes 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 was designed to give an edge to obtain job opportunity
in clinical research field.
||Available as self paced training (PIP, pure internet program)
Course Reading Material (chapters, PowerPoint presentations, Exercises, Quizzes & Final Exam)
|Career Opportunity Pathways
||Clinical Research Associate / Coordinator, Clinical Research Monitor, Trial Documentation Specialist,
CRA - Trial master File Maintenance, CRA - Trial Documents Validation and CRF Data
to download program brochure
||NJ Office - (P) 732.770.4100
Fax - 888.532.0210
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