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
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
This role will play a key role in bringing deep clinical understanding and judgment in benefit-risk assessments role will also ensure projects adhere to Good Clinical and Pharmacovigilance Practice and Regulatory interpretation of safety information collected from pre-clinical through to post-marketing, including medical review Investigator's Brochures, Clinical Study Protocol, Study Safety Plans, and Clinical Safety reports. Reviewing interpretation of safety information collected from pre-clinical through to post-marketing, including medical review
This role will play a key role in bringing deep clinical understanding and judgment in benefit-risk assessments role will also ensure projects adhere to Good Clinical and Pharmacovigilance Practice and Regulatory interpretation of safety information collected from pre-clinical through to post-marketing, including medical review Investigator's Brochures, Clinical Study Protocol, Study Safety Plans, and Clinical Safety reports. Reviewing interpretation of safety information collected from pre-clinical through to post-marketing, including medical review
facilities. Collaborate with health teams to establish clinical standards and procedures. Analyse current practices with DOH and the TB Technical Manager to conduct Clinical and Mortality Audits. Monitor availability and
including assisting in technical documentation and clinical evaluations. Deliver and coordinate training on
Responsible to manage and maintain the onsite medical clinic and facility, equipment and medical consumable including calibration of alcohol breathalyzer, all clinic equipment and health and safety department equipment records and the safekeeping thereof in the onsite clinic Handling all Department of Employment and Labour
Responsible to manage and maintain the onsite medical clinic and facility, equipment and medical consumable including calibration of alcohol breathalyzer, all clinic equipment and health and safety department equipment records and the safekeeping thereof in the onsite clinic Handling all Department of Employment and Labour
Participating in the development or implementation of clinical trial protocols to meet regulatory requirements
creating value for customers in life science and clinical diagnostics markets. Responsibilities Conceptualise