Senior Manager/Associate Director of Regulatory Affairs - Remote

Overview

The Senior Manager/Associate Director of Regulatory Affairs will assist in the development and implementation of regulatory strategies to advance Cogent’s precision kinase inhibitors in oncology and rare diseases. This individual will provide strategic input and regulatory support to cross-functional development teams. Working alongside senior Regulatory staff, this individual will be a key contributor to Cogent’s project and regulatory teams.

In Short

• Assist in the development of regulatory strategies.
• Implement regulatory strategies for precision kinase inhibitors.
• Provide strategic input to development teams.
• Support cross-functional teams in regulatory matters.
• Work alongside senior Regulatory staff.
• Contribute to project and regulatory teams.

Requirements

• Experience in regulatory affairs.
• Knowledge of oncology and rare diseases.
• Ability to work in cross-functional teams.
• Strong strategic thinking skills.

Benefits

• Opportunity to work on innovative therapies.
• Collaborative work environment.
• Professional development opportunities.