Job Description: The Clinical Research Associate (CRA) performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH GCP, FDA guidelines, local regulations and Sponsor’s SOPs. The CRA conducts site visits to assess protocol and regulatory compliance and manages required documentation and ensures that data will pass international quality assurance audits Job Requirements: Demonstrated clinical trial monitoring skills Excellent standard of verbal and written communication skills in English Medical, pharmaceutical or other life-science related degree Highly organized with strong attention to detail and deadlines At least 1 year of independent monitoring experience in a CRO, pharmaceutical or biotech company In-depth understanding of ICH/GCP guidelines Advanced skills across all of the Microsoft packages Job Details: Company: PPD Vacancy Type: Full Time Job Location: Johannesburg Application Deadline: N/A Apply Here instantcareers.net
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