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Responsible for the study drugs/consumables in the IMU;
Assist Study Teams in the areas of Investigational Products procurement, preparation, labelling and re-packaging for clinical trial use;
Responsible for all regulatory/ethics audits pertaining to investigational products;
Develop relevant SOPs for the handling & management of Investigational Products;
Prepare protocols /protocol amendments/ IB/ clinical study reports in collaboration with other appropriate functions;
Research, write, edit and proof copy to the highest standard (scientific and grammatical) for a full range of medical education and communications materials;
Provide medical editing review of draft and final documents prepared by other team members before internal or external distribution;
Manage and coordinate materials through design/production to print-ready stage;
Serve as the primary client contact under departmental supervision;
Provide medical information supports to CRCs.
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