Key Role responsibility

• Develop a CI tool to facilitate proactive API portfolio management.
• Review, compile and organize the existing assessment data into a structured repository, liaising closely with Medical Affairs Team.
• Coordination to consolidate work already done in one place in a simplified manner.
• Collaborate with cross-functional team SMEs, particularly in Medical, Safety/Toxicology, Clinical and Eco-Toxicology, for input, filling data-gap and validation. Incorporate feedback and refine the tool accordingly.
• Run ad-hoc literature searches as necessary.
• Support Global and Local teams in identifying pipeline opportunities.
• Coordinate with relevant stakeholders for tool access and usage.
• Documentation outlining tool functionalities and usage guidelines.
• Stakeholder engagement plan for tool dissemination and support.

Why you?
Basic Qualifications:

• Bachelor's or Master's degree in Scientific disciplines such as Medical Sciences, Pharmacy, Pharmacology, Biology, Clinical Research, Biochemistry
• Maximum 25 years old

Preferred Qualifications:

• Ideally Regulatory / Medical/ Safety experience in academic or enterprise environment.
• Result-oriented, ability to problem-solve and to "connect-the-dots" among different scientific disciplines.