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
purpose of the job: To provide clinical expertise in support of clinical research activities, including according to the study protocol and providing clinical insight and support to the local investigator quality assurance of study file source data, i.e. clinical source notes and CRFs to ensure the forms are study Accurately abstract information from the clinical notes Make sure that all the NHLS results have Professional Nurse Advantageous: REDCap Training Good Clinical Practice Certificate (GCP) Any qualification in
purpose of the job: To provide clinical expertise in support of clinical research activities, including according to the study protocol and providing clinical insight and support to the local investigator quality assurance of study file source data, i.e. clinical source notes and CRFs to ensure the forms are study Accurately abstract information from the clinical notes Make sure that all the NHLS results have Professional Nurse Advantageous: REDCap Training Good Clinical Practice Certificate (GCP) Any qualification in
This role will play a key role in bringing deep clinical understanding and judgement in benefit-risk assessments 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 analysis. Providing expert safety input to the clinical development program for some Client projects while
This role will play a key role in bringing deep clinical understanding and judgement in benefit-risk assessments 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 analysis. Providing expert safety input to the clinical development program for some Client projects while
Medical Technician/Technologist Blood Transfusion or Clinical Pathology or Haematology or Medical Scientist
Medical Technician/Technologist Blood Transfusion or Clinical Pathology or Haematology or Medical Scientist