Senior Safety Strategist, Medical Science Lead, Global Risk Management

8 hours ago


Copenhagen, Copenhagen, Denmark Lundbeck AS, H Full time

We are seeking a highly skilled and experienced Senior Safety Strategist to join our team at Lundbeck A/S, H. As a key member of the Global Medical Safety department, you will play a critical role in developing and implementing safety strategies for our products.

Company Overview:

Lundbeck is a global pharmaceutical company dedicated to delivering innovative therapies that improve the lives of individuals with brain diseases. Our team of experts is passionate about advancing neuroscience research and developing treatments that make a meaningful difference in people's lives.

Salary:

The estimated annual salary for this position is approximately $120,000 - $180,000, depending on qualifications and experience. This compensation package includes a base salary plus performance-based bonuses and benefits.

About the Role:

This challenging position offers an exciting opportunity to work independently as well as collaboratively with various stakeholders and team members. As a Senior Safety Strategist, you will be responsible for setting the direction for safety evidence generation and risk minimization, planning and interpreting safety data analyses, benefit-risk assessments, and providing medical-scientific input to regulatory documents.

Your Key Responsibilities:

Strategically manage safety surveillance and risk minimization activities for assigned compounds/productsChair cross-functional Safety Committee(s) to set and change overall safety evidence generation and risk management strategyCollaborate with various stakeholders and team members to achieve shared goalsStay abreast of developments in neuroscience and patient safety fieldsEstablish network within the R&D organization

Requirements:

To succeed in this role, you must have:

  • A Master's degree in life sciences (e.g., MD, M.Sc. Pharmacy, M.Sc. Human Biology)
  • Solid medical-scientific knowledge and ability to make sound medical decisions
  • Solid experience (at least 8 years) within patient safety/pharmacovigilance and clinical development
  • Profound knowledge and understanding of medical concepts and scientific methodology
  • Excellent understanding of global PV regulatory environment

Benefits:

As a valued member of our team, you can expect a comprehensive benefits package, including access to training and development opportunities, flexible working arrangements, and a range of employee benefits. We also offer a dynamic and inclusive work environment that promotes collaboration, creativity, and innovation.

Contact Information:

If you are a motivated and results-driven professional with a passion for patient safety and medical science, we encourage you to apply for this exciting opportunity.


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