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Course Description:Clinical Research Monitoring and Coordination For those seeking qualifications to manage and conduct clinical trials, the course emphasizes practical and regulatory requirements essential to successful trial management. Included are key tips from industry experts to enhance your trial management abilitities. This course is essential to obtaining and advancing your career. As well, you will learn many real world and practical points in successful trials.
The American Nurses' Credentialing Center Commision has accredited this course for 33 contact hours for Nursing Continuing Education Units (CEUs).
You will be allocated up to 3 months to complete the 10 chapters and 2 open book exams based on CD lecture series and coordinated slide presentation.
- Describe key steps in the Drug Development process.
- Gain insight to managing roles/opportunities in Clinical Research.
- Identify ethical issues in clinical research.
- Evaluate the development of new products.
- Institute and obtain proper Informed Consent for all types of study subjects.
- Understand the latest Good Clinical Practices as applied to medical research.
- Learn to employ efficient and appropriate study subject recruitment methods.
- Develop a suitable clinical trial protocol and study budget.
- Identify product adverse effects and proper reporting requirements.
- Develop qualifications sought by the Pharmaceutical, Biotech & Medical Device industries