coordinate the approval of a member's chronic medicine and to ensure that he/ she has access to this treatment within the available scheme benefit and medicine formulary. To participate in the clinical review motivation for exceptional funding for non-formulary medicines and to engage with various stakeholders – both prescriptions in accordance with the relevant medicine formulary. Lower healthcare costs through DUR drug interactions between disease conditions and medicine. Assist with treatment counselling and disease
coordinate the approval of a member's chronic medicine and to ensure that he/ she has access to this treatment within the available scheme benefit and medicine formulary. To participate in the clinical review motivation for exceptional funding for non-formulary medicines and to engage with various stakeholders – both prescriptions in accordance with the relevant medicine formulary. Lower healthcare costs through DUR drug interactions between disease conditions and medicine. Assist with treatment counselling and disease
the relevant medicine Regulatory Authorities (Country Specific where applicable), Medicines and Related experience in Regulatory Affairs, preferably in human medicines Demonstrable experience across the product development
guidelines pertaining to the Wholesale license for medicinal products and Good Wholesaling/Distribution and storage, packaging, supplying or selling of any medicine or schedule substance or the supervision thereof
guidelines pertaining to the Wholesale license for medicinal products and Good Wholesaling/Distribution and storage, packaging, supplying or selling of any medicine or schedule substance or the supervision thereof
To ensure legal compliance with the relevant Medicine Regulatory Authorities (Country Specific where
Excellent communication and interpersonal skills, both oral and written. Exceptional organizational and time