Обязанности и достижения:
Clinical Research
Supervision of Clinical research activities, including phase III-IV clinical trials, Investigator initiated studies, and post-marketing observational projects. Budget management.
Preparation, review and approval of local clinical studies, CRO management.
Medical Affairs:
Review & approval of promotional materials and local scientific publications; Medical Information co-ordination & field force training; Regulatory activities related to clinical research and reimbursement programs.
Pharmacovigilance:
Safety surveillance/reporting/Training.
Quality Assurance
Department audit management (audit co-ordination), Evaluation of local manufacturing Sites (co-audit).