apply for the Independent Contractor position of Clinical Evaluator to be based at Beier Drawtex Healthcare for preparing Clinical Evaluation Plans, Clinical Evaluation Reports, Post Market Clinical Follow Up Reports other clinical documentation as required for CE marked devices Responsible for writing Clinical Investigation Investigation Plans Provide clinical input into product development projects Consistently provide feedback feedback on updates to clinical regulatory requirements and related standards / guidelines Relevant medical
apply for the Independent Contractor position of Clinical Evaluator to be based at Beier Drawtex Healthcare for preparing Clinical Evaluation Plans, Clinical Evaluation Reports, Post Market Clinical Follow Up Reports other clinical documentation as required for CE marked devices Responsible for writing Clinical Investigation Investigation Plans Provide clinical input into product development projects Consistently provide feedback feedback on updates to clinical regulatory requirements and related standards / guidelines Relevant medical
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
Vaccines and Infectious Diseases Analytics (VIDA) Research Unit of the University of the Witwatersrand, formerly formerly RMPRU (Respiratory and Meningeal Pathogens Research Unit) has for over 20 years conducted numerous information: Wits VIDA Research Unit conducts cutting-edge scientific research The Unit aims to save lives middle-income countries through translational research that informs local and global policy recommendations next-generation and novel vaccines Wits VIDA's research is focused on the clinical and molecular epidemiology of vaccine-preventable
Vaccines and Infectious Diseases Analytics (VIDA) Research Unit of the University of the Witwatersrand, formerly formerly RMPRU (Respiratory and Meningeal Pathogens Research Unit) has for over 20 years conducted numerous information: Wits VIDA Research Unit conducts cutting-edge scientific research The Unit aims to save lives middle-income countries through translational research that informs local and global policy recommendations next-generation and novel vaccines Wits VIDA's research is focused on the clinical and molecular epidemiology of vaccine-preventable
a legal framework within which to operate the research and other activities necessary to support its epidemiological, clinical, and basic science research and innovation It currently manages several clinical trials trials and research projects As part of ongoing core and nested work, the Division seeks to appoint a qualified ensure high data quality Monitor the progress of research activities and generate regular and ad-hoc reports Maintain study site documentation following Good Clinical Practice Assist with any outstanding ethics application
a legal framework within which to operate the research and other activities necessary to support its epidemiological, clinical, and basic science research and innovation It currently manages several clinical trials trials and research projects As part of ongoing core and nested work, the Division seeks to appoint a qualified ensure high data quality Monitor the progress of research activities and generate regular and ad-hoc reports Maintain study site documentation following Good Clinical Practice Assist with any outstanding ethics application
health-focused epidemiological, clinical, and basic science research and innovation