Are you a skilled Clinical Technologist with expertise in sonars and cath lab procedures? Our esteemed requirements:
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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
Please note that we are an immigration company and do charge a facilitation fee. We are accredited by OMARA, a branch of the Department of Immigration and Border Protection in Australia. For a Free Eligibility assessment please apply online, contact 27 21 201 1551 or follow the link to complete a fr
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
Medical Technician/Technologist Blood Transfusion or Clinical Pathology or Haematology or Medical Scientist Circumstances Provide 24-hour technical support and consultation to stakeholders if required. National / international
Medical Technician/Technologist Blood Transfusion or Clinical Pathology or Haematology or Medical Scientist Circumstances Provide 24-hour technical support and consultation to stakeholders if required. National / international
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