Are you a skilled Clinical Technologist with expertise in sonars and cath lab procedures? Our esteemed requirements:
job:
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
job:
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
and calibration of equipment
Clinical Trials, Observational Studies, and Fundamental
and providing support to Monitors, Clinical Trial Coordinators, Clinic staff, and Laboratory staff to facilitate
facilitate the smooth running of Clinical Trials at the site level