Manage, negotiate and advise on complex legal and business transactions including agreements relating to research collaborations, technology licensing, commercial licensing, manufacturing process development and technology transfer.
Monitor toxicology studies for appropriate conduct, accuracy and timely execution; audit raw data for accuracy, review draft reports and finalize them as submission-ready documents for regulatory authorities.
Overall strategic leader for product development/early development projects. Set the overall vision and direction for the project and serve as visible project champion and focal point for critical project information.
The successful candidate can demonstrate impact on drug discovery projects, independently manage the technical and strategic needs of projects, design and execute experiments that enable decision making and troubleshoots and solves technical and logistical challenges.