The Clinical Laboratory Operations QA Associate I reports to the Lead Clinical Laboratory Operations Laboratory Operations of specimen processing for HVTN clinical trials across Southern Africa. A person in this coordinate and facilitate clinical site specimen processing and clinical testing laboratory projects Division of AIDS or DAIDS contractors. Manage clinical site laboratory supply program including resourcing teams that support the implementation of HVTN clinical trials in Southern Africa. Other duties and assignments
for developing novel technologies that promote research and improve human health. Watchmaker Genomics Development Group and will involve support of a research program aimed at developing and characterising science and clinical diagnostics markets. Responsibilities Conceptualise and champion research projects to drive impactful and relevant biotechnology research, with the objective of developing products of record of successfully proposing and executing research projects. Excellent organisational skills and
You've gained experience doing manager research and you're keen to join a business where you can directly PM's Is this you? You've got what it takes to research asset managers and know how to identify good performance in an Analyst role where you have done manager research. Attention to detail, effective communication
expertise. As a Senior Manager Research Analyst, you'll provide key manager research analysis which will be used dynamic investment team. ✔️ Minimum 5 years manager research experience within the multi-manager, fund of funds
to participate in a Generic Management NQF 3 Learnership. Qualification: Generic Management NQF 3 Potential
to participate in a Generic Management NQF 3 Learnership. Qualification: Generic Management NQF 3 Potential
Clinical Risk Management Specialist Industry: Insurance Location: Cape Town Type: Hybrid (3 In/ 2 Out) seeks to employ a Clinically qualified individual to assist within their Clinical Risk Management team address risk profiles. Provide clinical leadership and support. Analyze research data. Requirements : Registered the relevant council. Proven underwriting and clinical risk management working experience within Managed Managed Care or Insurance Industry. Research experience highly advantageous. Proficiency in MS Word, Excel
Clinical Risk Management Specialist Industry: Insurance Location: Cape Town Type: Hybrid (3 In/ 2 Out) seeks to employ a Clinically qualified individual to assist within their Clinical Risk Management team address risk profiles. Provide clinical leadership and support. Analyze research data. Requirements : Registered the relevant council. Proven underwriting and clinical risk management working experience within Managed Managed Care or Insurance Industry. Research experience highly advantageous. Proficiency in MS Word, Excel
Provide clinical inputs on ex-gratia funding requests Open, review and resolve all clinical queries and and assessments through providing a clinical decision or requesting more information where required Implement authorisation and claiming is facilitated Provide clinical training / support to identified stakeholders is shared as required and maintained within the research library Provide advice and / or training as required Knowledge and application of clinical principles and processes Knowledge of clinical and funding protocol development
Provide clinical inputs on ex-gratia funding requests Open, review and resolve all clinical queries and and assessments through providing a clinical decision or requesting more information where required Implement authorisation and claiming is facilitated Provide clinical training / support to identified stakeholders is shared as required and maintained within the research library Provide advice and / or training as required Knowledge and application of clinical principles and processes Knowledge of clinical and funding protocol development