Chief Medical Documentation Officer

3 days ago


Copenhagen, Copenhagen, Denmark Lundbeck AS, H Full time
Medical Documentation Leadership Role

This is an exciting opportunity to lead the Medical Documentation department at Lundbeck A/S, H. As the Head of Global Regulatory Affairs and R&D Quality, you will be responsible for driving digital transformation and enhancing R&D productivity through change management initiatives, implementation of innovative digital platforms, and upskilling team members.

The successful candidate will foster cross-functional collaboration to optimize regulatory submission processes, ensuring efficiency in time, resource allocation, and quality. You will provide state-of-the-art medical writing expertise to support Global Clinical Development and regulatory strategies for both development projects and marketed products.

In this role, you will be responsible for ensuring effective resource and budget planning to achieve our strategic goals while maintaining the highest quality standards, including oversight of outsourced tasks. You will work closely with the team to create a positive and productive work environment that encourages innovation and collaboration.

We are looking for a proactive, cross-functional collaborator with an inspiring strategic mindset. You should have experience with digital transformation of medical documentation and a strong understanding of digital technologies. The ability to support, inspire, and motivate a highly competent medical writing team is critical. You will thrive in building high-performance teams and serve as a sparring partner to your employees and stakeholders.



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