Post type:-Diploma
The demand has never been greater for professionals who can help companies ensure compliance with applicable laws and regulations in the development and commercialization of new drugs and healthcare products. The Clinical Research, Pharmacovigilance and Regulatory Affairs program will provide you with knowledge and insight into the most recent developments in the clinical research, pharmacovigilance and regulatory affairs field.
careers in the field of Clinical Research and Pharmacovigilance:
- Clinical Research Coordinator
- Pharmacovigilance data management Associate
- Clinical Research Associate
- Pharmacovigilance Associate
- Clinical Data Management Associate
- Clinical Research Project Leader
- Pharmacovigilance Project leader
- Clinical Research Monitor
- Medical Information Associate
- Pharmacovigilance Officer
- Quality Control in Clinical Research
- Quality Assurance in Clinical Research
- Quality Assurance in Pharmacovigilance
- Auditor in Clinical Research and Pharmacovigilance
Requirements:-
- Hold a degree in “Clinical Research” from an Associate, Undergraduate, or Graduate Degree Program AND
- Have completed a minimum of one year of full-time experience (or 1,750 hours part-time) during the past two years as a Clinical Research Professional
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