Associate Director in RA CMC Semaglutide overseeing projects and leading teams in regulatory compliance. Working to define strategies for Semaglutide products at Novo Nordisk.
Responsibilities
Lead the team in employee development and resource utilization
Coordinate task prioritization for all team members
Clarify team direction and strategy
Responsible for Occupational Health & Safety in the team
Ensure quality and compliance of work processes
Requirements
Master’s degree or PhD in life science or similar
Professional proficiency in English
+8 years drug development experience
At least 3 years in leadership position
Experience in late-stage projects or LCM phase
Proven track record in leadership, project management
Out-of-box thinking and hands-on experience in high complexity tasks
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