healthcare sector; Keeping up to date with the latest clinical data supplied by the company, and interpreting interpreting, presenting and discussing this data with health professionals during face-to-face interactions. Maintaining attending training sessions; reviewing published clinical trials; attending scientific meetings. Adjusting and patient's needs and presenting appropriate clinical data to increase awareness of products whilst patients ‘needs; Collaborating with the Medical Department to plan and execute educational/scientific activities
healthcare sector; Keeping up to date with the latest clinical data supplied by the company, and interpreting interpreting, presenting and discussing this data with health professionals during face-to-face interactions. Maintaining attending training sessions; reviewing published clinical trials; attending scientific meetings. Adjusting and patient's needs and presenting appropriate clinical data to increase awareness of products whilst patients ‘needs; Collaborating with the Medical Department to plan and execute educational/scientific activities
and medicine formulary. To participate in the clinical review of existing treatment and, where appropriate loading of authorisations. Prepare complex cases for clinical review for exceptional funding by the medical the 27 chronic disease list (CDL) conditions and clinical criteria requirements for each condition. Computer
and medicine formulary. To participate in the clinical review of existing treatment and, where appropriate loading of authorisations. Prepare complex cases for clinical review for exceptional funding by the medical the 27 chronic disease list (CDL) conditions and clinical criteria requirements for each condition. Computer
needed to drive performance in their respective departments. Robust mitigation plans in place to engage. , LRMP Labelling and Artwork Management Robust Health Authority interactions To track and manage all Marketing Authorization Applications to the SA Health Authority according to SA HA guidelines and GRP cross-functional departments. Health Authority interactions: All communication with Health Authorities regarding Extent of compliance of submissions with SOP's and Health Authority guidelines. Accuracy of content of documentation
strategies are defined and executed and Board of Health requirements are met, ensuring a submission ready Understanding of the pharmaceutical industry, clinical trials, and pharmacovigilance Knowledge and understanding
registration of medicines with the South African Health Products Regulatory Authority and the maintenance Responsible and accountable to the South African Health Products Regulatory Authority and the South African provide insight into RA activities and report on department progress. Form part of the global Senior Leadership
registration of medicines with the South African Health Products Regulatory Authority and the maintenance Responsible and accountable to the South African Health Products Regulatory Authority and the South African provide insight into RA activities and report on department progress. Form part of the global Senior Leadership
management level Sound understanding of Safety, Health and Environment Ensure team compliance with the
for Cycle Meetings. Together with the Training Department develop training activities for Medical Reps