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, the management and analysis of data and the preparation of manuscripts for publication. The role will also be responsible for: Contributing to the research project by collaborating with the Research Team
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, and biomarker analysis from human biospecimens. Working under the broad direction of the Chief Investigator, you’ll contribute to project design, data analysis, and manuscript preparation, while
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Investigator and team on study design, data analysis, ethics applications, and academic publications. The role also involves engaging with partner sites, maintaining stakeholder relationships, supporting
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administrators, and patient advocates—who bring deep domain knowledge without necessarily having technical expertise. You will play a key role in designing and implementing research projects, analysing data, and
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at improving the quality, safety, and effectiveness of medication use across the reproductive lifespan. The role involves managing and analysing data from clinical trials, cohort studies, and large linked
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initiatives under the guidance of the Centre Director. This position involves leading and managing a range of NCETA’s projects, overseeing data collections and datasets, and providing expert methodological
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Information You are required to submit your CV and a Suitability Statement of no more than 3 pages, addressing the Key Position Capabilities of the Position Description. For more information regarding this
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activities including project management, stakeholder engagement, data collection and analysis, and the development of written outputs for both community organisations and peer-reviewed journals. The Research
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are strongly recommended to be fully vaccinated against COVID-19 in line with the SA Health policy. How to Apply and Information You are required to submit your CV and a Suitability Statement of no