technical reports to IRBs, SAHPRA, and sponsors as needed Update site delegation logs when new staff join responsibilities defined in site delegation logs per qualifications and training Develop and/or review study-specific Degree in Health Care or Life Sciences GCP qualification A recognized Quality Control Course (for clinical Internet Required minimum work experience: 3 years of quality control experience in a clinical trial environment least 5 years experience working in clinical trials At least 2 years of regulatory experience Desirable additional
technical reports to IRBs, SAHPRA, and sponsors as needed Update site delegation logs when new staff join responsibilities defined in site delegation logs per qualifications and training Develop and/or review study-specific Degree in Health Care or Life Sciences GCP qualification A recognized Quality Control Course (for clinical Internet Required minimum work experience: 3 years of quality control experience in a clinical trial environment least 5 years experience working in clinical trials At least 2 years of regulatory experience Desirable additional
technical reports to IRBs, SAHPRA, and sponsors as needed
keeping, and the creation of audit files. QUALIFICATIONS AND EXPERIENCE A postgraduate degree in one of the management training and qualification. Substantial senior management experience, of at least 5 years with Demonstrable strategic, business acumen, and leadership experience in the relevant field. Knowledge and understanding
keeping, and the creation of audit files. QUALIFICATIONS AND EXPERIENCE A postgraduate degree in one of the management training and qualification. Substantial senior management experience, of at least 5 years with Demonstrable strategic, business acumen, and leadership experience in the relevant field. Knowledge and understanding
partner. The ideal candidate will have extensive experience with SAICA, a strong background in audit planning
Qualifications: