3 Clinical Trials Associate Jobs
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Clinical Document Quality Specialist II South Africa Implement and administer Ora document management systems (Veeva Vault) and related procedures that allow Ora staff to capture, store, retrieve, share, and destroy electronic records and documents in a... More than 30 days ago
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Associate Project Manager Thermo Fisher Scientific - Gauteng, SA Assist in maintaining FCS SA’s Quality System in compliance with Fisher Clinical Services’ approved procedures and policies, cGxP and regulatory requirements as applicable when leading the day to day activities... Not specified More than 30 days ago
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Clinical Research Coordinator Rondebosch Review of study files with the sponsor delegate.Drawing up and designing templates for the source documents used by the investigators according to specific protocol requirements.Site must at all times... 2 days ago
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