Clinical Trail Researcher required for Institute in Cape Town. Clinical Trail Researcher required for
Clinical Trail Researcher required for Institute in Cape Town. Clinical Trail Researcher required for
The Clinical Laboratory Operations QA Associate I reports to the Lead Clinical Laboratory Operations Operations QA Associate , and is responsible for creating, developing, monitoring and managing quality systems Laboratory Operations of specimen processing for HVTN clinical trials across Southern Africa. A person in this results. The Quality Assurance Associate has additional responsibilities in leading project efforts and management for the HVTN QA Associate I is to provide oversight, coordinate and facilitate clinical site specimen processing
The Clinical Laboratory Operations QA Associate I reports to the Lead Clinical Laboratory Operations Operations QA Associate , and is responsible for creating, developing, monitoring and managing quality systems Laboratory Operations of specimen processing for HVTN clinical trials across Southern Africa. A person in this results. The Quality Assurance Associate has additional responsibilities in leading project efforts and management for the HVTN QA Associate I is to provide oversight, coordinate and facilitate clinical site specimen processing
Institute (Wits RHI) is a renowned African-led research institute that seeks solutions to Africa's health purpose of the job: Day-to-day coordination of research-related activities including quality data collection critical curiosity, and a neutral tone Compile research summaries and reports Perform quality data capture stakeholders Participation in all appropriate research-related meetings (internal and external) and providing corrected, initialed, and dated Comply with Good Clinical Practice (GCP), Protocol Standard Operating Procedures
Institute (Wits RHI) is a renowned African-led research institute that seeks solutions to Africa's health purpose of the job: Day-to-day coordination of research-related activities including quality data collection critical curiosity, and a neutral tone Compile research summaries and reports Perform quality data capture stakeholders Participation in all appropriate research-related meetings (internal and external) and providing corrected, initialed, and dated Comply with Good Clinical Practice (GCP), Protocol Standard Operating Procedures
job:
Reference: PE000962-CP-1 Our client is looking for an Associate to join their firm. Requirement Matric Minimum articles Job duties Legal Research and Analysis : Conducting thorough legal research on various issues and
/>Legal Research and Analysis:
Conducting thorough legal research on various issues
Minimum requirements: