Global Regulatory Affairs Associate Director (Cardio-Metabolic)
Novartis
Global Regulatory Affairs Associate Director (Cardio-Metabolic)
Job Description
Summary
Summary Office Location: London (The Westworks), United Kingdom#LI-Hybrid Hybrid (12 days per month on-site if living within 50 miles to our London office)
#LI-Remote Remote (if living beyond 50 miles to our London office)
Internal Job Title: Global Program Regulatory Associate Director
We are looking for an experienced and proactive Global Regulatory Affairs Associate Director Cardio-Metabolic to join our Global Regulatory Affairs team.The role involves directing the development and submission of regulatory documents, providing strategic direction and negotiating with agencies to expedite approvals. It also ensures timely approval and compliance of new and marketed products, and serves as a regulatory liaison throughout the product lifecycle.
Locations
- Home Worker, United Kingdom
Salary
Estimated Salary Rangemedium confidence
50,000 - 85,000 GBP / yearly
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Regulatory affairs strategyintermediate
- Document development and submissionintermediate
- Agency negotiationintermediate
- Compliance managementintermediate
- Strategic direction provisionintermediate
- Proactivityintermediate
Required Qualifications
- Experienced in Global Regulatory Affairs (experience)
- Expertise in Cardio-Metabolic area (experience)
Responsibilities
- Direct development and submission of regulatory documents
- Provide strategic direction and negotiate with agencies to expedite approvals
- Ensure timely approval and compliance of new and marketed products
- Serve as regulatory liaison throughout the product lifecycle
- Join Global Regulatory Affairs team as Associate Director
Answer 10 quick questions to check your fit for Global Regulatory Affairs Associate Director (Cardio-Metabolic) @ Novartis.
10 Questions
~2 Minutes
Instant Score
Global Regulatory Affairs Associate Director (Cardio-Metabolic)
Novartis
Global Regulatory Affairs Associate Director (Cardio-Metabolic)
Job Description
Summary
Summary Office Location: London (The Westworks), United Kingdom#LI-Hybrid Hybrid (12 days per month on-site if living within 50 miles to our London office)
#LI-Remote Remote (if living beyond 50 miles to our London office)
Internal Job Title: Global Program Regulatory Associate Director
We are looking for an experienced and proactive Global Regulatory Affairs Associate Director Cardio-Metabolic to join our Global Regulatory Affairs team.The role involves directing the development and submission of regulatory documents, providing strategic direction and negotiating with agencies to expedite approvals. It also ensures timely approval and compliance of new and marketed products, and serves as a regulatory liaison throughout the product lifecycle.
Locations
- Home Worker, United Kingdom
Salary
Estimated Salary Rangemedium confidence
50,000 - 85,000 GBP / yearly
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Regulatory affairs strategyintermediate
- Document development and submissionintermediate
- Agency negotiationintermediate
- Compliance managementintermediate
- Strategic direction provisionintermediate
- Proactivityintermediate
Required Qualifications
- Experienced in Global Regulatory Affairs (experience)
- Expertise in Cardio-Metabolic area (experience)
Responsibilities
- Direct development and submission of regulatory documents
- Provide strategic direction and negotiate with agencies to expedite approvals
- Ensure timely approval and compliance of new and marketed products
- Serve as regulatory liaison throughout the product lifecycle
- Join Global Regulatory Affairs team as Associate Director
Answer 10 quick questions to check your fit for Global Regulatory Affairs Associate Director (Cardio-Metabolic) @ Novartis.
10 Questions
~2 Minutes
Instant Score