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
procurement, and stock in the clinic Lead the clinic team to ensure that all clinical trials are conducted in within the clinic Troubleshoot daily clinic operational issues in collaboration with the clinical operations comprehensive support of all operational aspects of clinical trials including overall delivery of protocol measure related initiatives in collaboration with the clinic operations manager Oversee maintenance and deployment/use related guidelines, etc.) in collaboration with the clinic operations manager Enforce organizational standard
procurement, and stock in the clinic Lead the clinic team to ensure that all clinical trials are conducted in within the clinic Troubleshoot daily clinic operational issues in collaboration with the clinical operations comprehensive support of all operational aspects of clinical trials including overall delivery of protocol measure related initiatives in collaboration with the clinic operations manager Oversee maintenance and deployment/use related guidelines, etc.) in collaboration with the clinic operations manager Enforce organizational standard
participants from local clinics and surrounding hospitals for participation in a clinical trial To assist with Maintaining a good working relationship with local clinic staff To do study-related duties as specified by minimum work experience: 2 Years' experience in the Clinical Research field Professional body registration: work experience, and personal abilities: Good Clinical Practice/Human Subject Protection certification
participants from local clinics and surrounding hospitals for participation in a clinical trial To assist with Maintaining a good working relationship with local clinic staff To do study-related duties as specified by minimum work experience: 2 Years' experience in the Clinical Research field Professional body registration: work experience, and personal abilities: Good Clinical Practice/Human Subject Protection certification
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
Ensure the site is well prepared for external lab, clinical, social science, and community monitoring reviews Assess staff awareness and compliance to Good Clinical Practice (GCP), Protocol requirements, Standard 1-2 years of relevant work experience within a clinical research environment in Quality Control and Quality of the relevant studies and SOPs, knowledge of clinical research documentation Computer literate with
job: To provide best practice data collection, clinical assessments, collection of specimens, and care medical notes and complete CRFs Maintain full clinical records for all participants Maintain an inventory nursing experience in STI/HIV, research and or clinical trials Professional body registration: South African similar will be an advantage Certification in good clinical practice Experience in a research environment