purpose of the job:
advantageous
Significant experience of regulatory drug development, manufacture, commercialisation or equivalent
/>Knowledge of regulatory procedures and legislation for drug development, product registration, line extension
/>Knowledge of regulatory procedures and legislation for drug development, product registration, line extension
documentation and investigations Support Adverse Drug Reaction (ADR) cases Conduct Root Cause Analysis
documentation and investigations Support Adverse Drug Reaction (ADR) cases Conduct Root Cause Analysis
Ability to pass background checks and drug screenings as required by the company and regulatory
the review of new/revised safety regulations (for drugs non-medicinal products & Medical Devices in familiarity with industry principles of product vigilance, drug development and pharmacology proficiency in Medical
the review of new/revised safety regulations (for drugs non-medicinal products & Medical Devices in familiarity with industry principles of product vigilance, drug development and pharmacology proficiency in Medical
Haematology. Within Transfusion, we have a few drugs but these are not really marketed and therefore
Clearance: Ability to pass background checks and drug screenings as required by the company and regulatory
organisations including Médecins sans Frontières (MSF), Drugs for Neglected Diseases initiations (DNDi) and community clinical procedures including dispensing of related drugs to study participants and other protocol related