Structure and secure strategic partnerships, licensing agreements and promotion agreements to exploit new business opportunities by developing proposals with thorough financial and qualitative analysis, negotiating key business terms, and driving to contract execution.

Candidate will be responsible for the conception and implementation of new research project ideas for the Lipocine Endocrine/Metabolic Disease area based upon an integration of biomedical knowledge, understanding of disease pathophysiology, current, and emerging medical practice, and commercial considerations.

Carry out pre-formulation required for the assessment of “developability” of an API, including solution and solid-state characterization studies, solubility/solubility enhancement studies, compatibility studies, polymorph and salt screening and characterization, particle size analysis, assessment of bulk properties of powders etc. Design and execute detailed experiments developing formulation and manufacturing process under QbD principles and transferring these methods and processes to drug product manufacturers.

Structure and secure strategic partnerships, licensing agreements and promotion agreements to exploit new business opportunities by developing proposals with thorough financial and qualitative analysis, negotiating key business terms, and driving to contract execution.