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
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
CONTRACT
EMAVUNDLENI CLINICAL RESEARCH SITE; CROSSROADS
The Desmond carry out laboratory activities at Emavundleni Clinical Research Site, as well as to ensure that the final of health and safety regulations
Advantageous:
with the performance of clinical trial-related duties in line with Good Clinical Practice (GCP) standards areas: Conduct Quality Control activities for clinical trials, assist with regulatory communications qualification A recognized Quality Control Course (for clinical trials) Computer literacy at a higher level including experience in a clinical trial environment At least 5 years experience working in clinical trials At least
with the performance of clinical trial-related duties in line with Good Clinical Practice (GCP) standards ul>
with the performance of clinical trial-related duties in line with Good Clinical Practice (GCP) standards areas: Conduct Quality Control activities for clinical trials, assist with regulatory communications qualification A recognized Quality Control Course (for clinical trials) Computer literacy at a higher level including experience in a clinical trial environment At least 5 years experience working in clinical trials At least