Our client a sustainable social solutions company is looking for a social scientist to provide specialist consulting services to clients in the areas of Social and Labour Plans, Mining Charter implementation services (specialising in no less than three): Social and Labour Plans (development and compliance reporting) Processes) Baseline Socio-Economic Study Surveys Social Impact Assessments Sustainable Development Action analysis and reporting of social science activities related to field of work. Develop findings, provide
Our client a sustainable social solutions company is looking for a social scientist to provide specialist consulting services to clients in the areas of Social and Labour Plans, Mining Charter implementation services (specialising in no less than three): Social and Labour Plans (development and compliance reporting) Processes) Baseline Socio-Economic Study Surveys Social Impact Assessments Sustainable Development Action analysis and reporting of social science activities related to field of work. Develop findings, provide
submission to the study coordinator/leadership team Assist in patient recruitment, screening, enrolment, and 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 equivalent Required minimum work experience: None Desirable additional education, work experience, and personal and/or exposure to clinical trial working environment Able to work independently and as part of a multi-disciplinary
submission to the study coordinator/leadership team Assist in patient recruitment, screening, enrolment, and 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 equivalent Required minimum work experience: None Desirable additional education, work experience, and personal and/or exposure to clinical trial working environment Able to work independently and as part of a multi-disciplinary
which the appointed person may be called on to assist with. Conducts research and produce research reports Embraces an action orientated approach to research and assist the team in developing appropriate interventions including social science and humanities, if interests and experience align. 3-5 years' working experience
which the appointed person may be called on to assist with. Conducts research and produce research reports Embraces an action orientated approach to research and assist the team in developing appropriate interventions including social science and humanities, if interests and experience align. 3-5 years' working experience
external lab, clinical, social science, and community monitoring reviews Assist in the completion of corrective corrective action for monitoring reviews Assist/ensure completion of corrective action for internal monitoring documentation available and up to date across all studies Assist with the review and revision of standard operating ensure that quality and productivity standards of own work are consistently and accurately maintained Maintain Health-related field Required minimum work experience: Minimum 1-2 years of relevant work experience within a clinical
external lab, clinical, social science, and community monitoring reviews Assist in the completion of corrective corrective action for monitoring reviews Assist/ensure completion of corrective action for internal monitoring documentation available and up to date across all studies Assist with the review and revision of standard operating ensure that quality and productivity standards of own work are consistently and accurately maintained Maintain Health-related field Required minimum work experience: Minimum 1-2 years of relevant work experience within a clinical
clinical trial to ensure protocol and GCP compliance Assist study team with efficient study start-up, conduct missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor, and regulatory correctly per protocol within the scope of practice Assist in patient recruitment, screening, and enrolment visits/audits or similar Manage procurement for the study Assist team members and support teams with an open helpful attitude, perform on-the-job training where necessary Assist the team with ad hoc assignments and duties as
clinical trial to ensure protocol and GCP compliance Assist study team with efficient study start-up, conduct missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor, and regulatory correctly per protocol within the scope of practice Assist in patient recruitment, screening, and enrolment visits/audits or similar Manage procurement for the study Assist team members and support teams with an open helpful attitude, perform on-the-job training where necessary Assist the team with ad hoc assignments and duties as