Are you a skilled Clinical Technologist with expertise in sonars and cath lab procedures? Our esteemed requirements:
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:
epidemiological, clinical, and basic science research and innovation It currently manages several clinical trials Maintain study site documentation following Good Clinical Practice Assist with any outstanding ethics application the public health sector Experience managing a clinical trial Good data management skills Able to work
epidemiological, clinical, and basic science research and innovation It currently manages several clinical trials Maintain study site documentation following Good Clinical Practice Assist with any outstanding ethics application the public health sector Experience managing a clinical trial Good data management skills Able to work