Onsite Associate Director – RA CMC Semaglutide

Posted yesterday

Apply now

About the role

  • 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

Benefits

  • Health & Safety compliance
  • Employee development
  • Team collaboration opportunities

Job title

Associate Director – RA CMC Semaglutide

Job type

Experience level

Senior

Salary

Not specified

Degree requirement

Postgraduate Degree

Location requirements

Report this job

See something inaccurate? Let us know and we'll update the listing.

Report job