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 in General Nursing (3 Years) Required minimum work experience: Minimum of 1 year of nursing experience research and or clinical trials Professional body registration: South African Nursing Council (SANC) in in General Nursing Desirable additional education, work experience, and personal abilities: Advanced
coordinator/leadership team Assist in patient recruitment, screening, enrolment, and retention of eligible according to protocol requirements as and when required Assist with stock-take for the project, ensuring stock maintained and low stock is flagged for procurement Assist the team with ad hoc assignments and duties as abilities: Research Internships and/or exposure to clinical trial working environment Able to work independently
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 in General Nursing (3 Years) Required minimum work experience: Minimum of 1 year of nursing experience research and or clinical trials Professional body registration: South African Nursing Council (SANC) in in General Nursing Desirable additional education, work experience, and personal abilities: Advanced
coordinator/leadership team Assist in patient recruitment, screening, enrolment, and retention of eligible according to protocol requirements as and when required Assist with stock-take for the project, ensuring stock maintained and low stock is flagged for procurement Assist the team with ad hoc assignments and duties as abilities: Research Internships and/or exposure to clinical trial working environment Able to work independently
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol all operations in the clinical trial to ensure protocol and GCP compliance Assist study team with efficient and missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor, and regulatory the scope of practice Assist in patient recruitment, screening, and enrolment of eligible patients according visits/audits or similar Manage procurement for the study Assist team members and support teams with an open helpful
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol all operations in the clinical trial to ensure protocol and GCP compliance Assist study team with efficient and missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor, and regulatory the scope of practice Assist in patient recruitment, screening, and enrolment of eligible patients according visits/audits or similar Manage procurement for the study Assist team members and support teams with an open helpful
for external lab, clinical, social science, and community monitoring reviews Assist in the completion completion of corrective action for monitoring reviews Assist/ensure completion of corrective action for internal documentation available and up to date across all studies Assist with the review and revision of standard operating 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
for external lab, clinical, social science, and community monitoring reviews Assist in the completion completion of corrective action for monitoring reviews Assist/ensure completion of corrective action for internal documentation available and up to date across all studies Assist with the review and revision of standard operating 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
Academics conducting these activities in order to assist with the management thereof. Description Main purpose 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
Academics conducting these activities in order to assist with the management thereof. Description Main purpose 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