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Counsel - Clinical Development, Medical & Regulatory Affairs
Novo Nordisk
Any Location, NJ
Category
Operations
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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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