Counsel - Clinical Development, Medical & Regulatory Affairs

Novo Nordisk
Any Location, NJ
Category Operations
Job Description
The position of Counsel - Clinical Development, Medical & Regulatory Affairs at Novo Nordisk is responsible for providing legal support to the Clinical Development, Medical & Regulatory Affairs (CMR) organization. The position will provide full lifecycle advice and counsel on matters relating to research and development, scientific exchange, and regulatory strategy and compliance.

Requirements

  • Juris Doctor (JD) degree or an internationally recognized equivalent and state bar admission
  • 5+ years of experience in a law firm or in-house legal department
  • Relevant experience providing legal advice to life sciences/pharmaceutical industry on research and development
  • In-depth knowledge of applicable state and federal laws and regulations
  • Demonstrated experience making and communicating risk assessments, identifying and resolving legal and regulatory issues, and making real-time decisions under pressure

Benefits

  • Medical, dental and vision coverage
  • Life insurance
  • Disability insurance
  • 401(k) savings plan
  • Flexible spending accounts
  • Employee assistance program
  • Tuition reimbursement program
  • Group legal insurance
  • Critical illness insurance
  • Identity theft protection
  • Pet insurance
  • Auto/home insurance
  • Sick time policy
  • Flexible vacation policy
  • Parental leave policy
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