for the deliverable of the Market Shaping output, manage all milestones, timelines, and any emerging interdependencies (donor) as relates to the market-shaping output work Manage the contractual relationship with CHAI and ensure monitoring of defined supply-side interventions Manage the contractual relationship with various drug drug manufacturers as relates to incentives Manage the day-to-day relationships with all stakeholders, in direction to the project Develop and effectively manage relationships with relevant Wits RHI structures
for the deliverable of the Market Shaping output, manage all milestones, timelines, and any emerging interdependencies (donor) as relates to the market-shaping output work Manage the contractual relationship with CHAI and ensure monitoring of defined supply-side interventions Manage the contractual relationship with various drug drug manufacturers as relates to incentives Manage the day-to-day relationships with all stakeholders, in direction to the project Develop and effectively manage relationships with relevant Wits RHI structures
job: The project manager/study coordinator is responsible for coordinating all clinical trial activities activities according to good clinical practice, the study protocol, and the site's standard operating procedures performance areas: Oversee all operations in the clinical trial to ensure protocol and GCP compliance Assist efficient study start-up, conduct, and close-out Manage regulatory updates throughout the study (New ICFs resolve protocol queries and missing data with Investigators and Clinical Trials Assistants Communicate with
of the job: To provide best practice data collection, clinical assessments, collection of specimens, Collect participant data from medical notes and complete CRFs Maintain full clinical records for all participants protocol and SOPs Prepare all relevant reports Capture data timeously and accurately Provide regular updates accountability for tasks and demonstrate effective self-management Follow through to ensure that quality and productivity nursing experience in STI/HIV, research and or clinical trials Professional body registration: South African
of the job: To provide best practice data collection, clinical assessments, collection of specimens, Collect participant data from medical notes and complete CRFs Maintain full clinical records for all participants protocol and SOPs Prepare all relevant reports Capture data timeously and accurately Provide regular updates accountability for tasks and demonstrate effective self-management Follow through to ensure that quality and productivity nursing experience in STI/HIV, research and or clinical trials Professional body registration: South African
Ensure the site is well prepared for external lab, clinical, social science, and community monitoring reviews report/s on findings for the site management team Support the Regulatory/Data team with periodic quality assurance Assess staff awareness and compliance to Good Clinical Practice (GCP), Protocol requirements, Standard accountability for tasks and demonstrate effective self-management Follow through to ensure that quality and productivity 1-2 years of relevant work experience within a clinical research environment in Quality Control and Quality
Ensure the site is well prepared for external lab, clinical, social science, and community monitoring reviews report/s on findings for the site management team Support the Regulatory/Data team with periodic quality assurance Assess staff awareness and compliance to Good Clinical Practice (GCP), Protocol requirements, Standard accountability for tasks and demonstrate effective self-management Follow through to ensure that quality and productivity 1-2 years of relevant work experience within a clinical research environment in Quality Control and Quality
visit projections and planning Review data to identify trends, data quality issues, and areas for improvement patient files and data entries (i.e., eCRF's, CRF's) Support the storage and archiving of data as per the SOP visits, audits, site inspections, and similar Support data clean-up activities resulting from assessments Ensure Participate in regular planning sessions with line manager and/or technical specialists Compile prescribed assignments and duties as needed, delegated by the line manager and within the scope of practice Support all relevant
visit projections and planning Review data to identify trends, data quality issues, and areas for improvement patient files and data entries (i.e., eCRF's, CRF's) Support the storage and archiving of data as per the SOP visits, audits, site inspections, and similar Support data clean-up activities resulting from assessments Ensure Participate in regular planning sessions with line manager and/or technical specialists Compile prescribed assignments and duties as needed, delegated by the line manager and within the scope of practice Support all relevant
activities, including analysis and interpretation of data, to conduct research relevant to the discipline tests
Laboratory Administration:
and report quality control issues to Laboratory Manager Required Minimum Education