Regulatory Affairs Clinical Trials Pharmacist

1 week ago


Johannesburg, South Africa Ultra Personnel Full time

Experience must include an in-depth knowledge of new and emerging Acts, Regulations and guidelines pertaining to the pharmaceutical industry.
Must have knowledge of clinical trial methodologies ICH/GCP, FDA and local country regulations.
Knowledge of clinical trial and regulatory requirements as pertaining to human medicines is a must.
Must have a proven ability to manage complex regulatory issues and consistently deliver to time, cost and quality standards.



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