About the Role
Responsibilities:
Contribute to the review, interpretation and communication of scientific data pertaining to the efficacy and safety of compounds in development.
Attends congress and reviews literature to develop and augment expertise in therapeutic area.
Help develop program strategy including the clinical development plan, product lifecycle plans, target product profiles and draft labels. Reviews competitive landscape and help identify and evaluate business development opportunities.
Responsible for providing focused scientific and clinical study support from start-up clinical study report (CSR).
Participate in scientific education of internal and external stakeholders on the pre-clinical ( mechanism of action, animal models) and clinical ( epidemiology, diagnosis, treatment) data relevant to program. Engage opinion leader interactions to build pipeline awareness and foster research collaborations.
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