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
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
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
preparation, packing, and dispatching of kits for clinical trials conducted by WDIH Location: WDIH – Braamfontein Must be Adaptable and reliable Understanding of Clinical Trials Ability to operate in a pressurized environment
preparation, packing, and dispatching of kits for clinical trials conducted by WDIH Location: WDIH – Braamfontein Must be Adaptable and reliable Understanding of Clinical Trials Ability to operate in a pressurized environment
epidemiology of vaccine-preventable diseases, and clinical development of life-saving vaccines Wits VIDA strategy, WITS VIDA's world-class laboratory, clinical trials facility, and significant observational sites including but not limited to: VIDA offices, clinical trials department, and allocated hospital spaces Temperature monitoring systems (e.g. for laboratory and clinical samples) Security: oversee security requirements business insights, and reporting skills Good Clinical Practice (GCP) knowledge (can obtain a certificate
epidemiology of vaccine-preventable diseases, and clinical development of life-saving vaccines Wits VIDA strategy, WITS VIDA's world-class laboratory, clinical trials facility, and significant observational sites including but not limited to: VIDA offices, clinical trials department, and allocated hospital spaces Temperature monitoring systems (e.g. for laboratory and clinical samples) Security: oversee security requirements business insights, and reporting skills Good Clinical Practice (GCP) knowledge (can obtain a certificate