Develop effective packaging and supply strategies maximizing available inventory by location and shelf life while minimizing waste; oversee clinical packaging activities, coordinate release of drug for clinical use.

Foster a collaborative culture interacting with Drug Discovery and Pre-clinical Development team during early stages of drug development. Analyze the initial enabling procedures and develop phase appropriate routes to efficient and scalable manufacturing of peptides, noncanonical amino acids and small molecules to support pre-clinical and clinical trials.

Conceptualize, develop, revise, and finalize nonclinical toxicology study designs, data analyses, reports and nonclinical sections for IND first-in-human submissions, as well as required other regulatory submissions to ensure US and ex-US compliance.