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
Clinical Trail Researcher required for Institute in Cape Town. Clinical Trail Researcher required for
Clinical Trail Researcher required for Institute in Cape Town. Clinical Trail Researcher required for
through public health-focused epidemiological, clinical, and basic science research and innovation
epidemiological, clinical, and basic science research and innovation It currently manages a number of clinical trials and nested work, it seeks to appoint a qualified Clinical Trial Assistant to participate in a number of as an HIV Counsellor or similar Experience in clinical trials would be advantageous Desirable additional and personal abilities: Certification in good clinical practice is advantageous Certificate/qualification
epidemiological, clinical, and basic science research and innovation It currently manages a number of clinical trials and nested work, it seeks to appoint a qualified Clinical Trial Assistant to participate in a number of as an HIV Counsellor or similar Experience in clinical trials would be advantageous Desirable additional and personal abilities: Certification in good clinical practice is advantageous Certificate/qualification
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:
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol performance areas: Oversee all operations in the clinical trial to ensure protocol and GCP compliance Assist queries and missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor minimum work experience: 3-5 years experience in clinical trials/research Desirable additional education
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol performance areas: Oversee all operations in the clinical trial to ensure protocol and GCP compliance Assist queries and missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor minimum work experience: 3-5 years experience in clinical trials/research Desirable additional education