PharmaRelations is looking for a Head of Regulatory Affairs Development to lead and further develop our Regulatory Affairs services in the drug development space. This is a Sweden-based position, and you will be part of the Regulatory Management Team, reporting to the Nordic Head of Regulatory Affairs based in Denmark. This is a unique opportunity to combine deep regulatory affairs expertise with leadership, business development and client advisory work in a highly entrepreneurial environment. As Head of Regulatory Affairs Development, you will play a key role in shaping the future of our service offerings while supporting innovative biotech and pharmaceutical companies in bringing new medicines from development through regulatory approval. The role includes some travel within the Nordic countries. If you are not based within commuting distance of our Solna office, you should be comfortable travelling to the office a couple of times per month.
About PharmaRelations
PharmaRelations is the leading Nordic Life Science consulting partner, connecting expertise, talent and organizations across the pharmaceutical, biotech and medical technology industries. What many of us appreciate most about working at PharmaRelations is our entrepreneurial culture, short decision-making paths and the genuine opportunity to influence both the business and your own development. We believe in empowering our leaders to take initiative, challenge existing ways of working and contribute to the continued growth of the organization. This role offers a unique opportunity to shape and further develop our Regulatory Affairs Development offering, while building client relationships and driving commercial growth.
The Role
This is a multifaceted leadership role combining regulatory affairs expertise, strategic advisory work, customer engagement and business development. You will lead and further develop our Regulatory Affairs Development team while supporting clients with strategic regulatory affairs guidance throughout the drug development lifecycle.
The role will include:
The role will initially combine leadership responsibilities with hands-on client work and consulting assignments.
Your Background
We are looking for a senior regulatory affairs professional with extensive experience in clinical stage Regulatory Affairs work and a strong understanding of the tasks and challenges in global drug development.
You likely bring:
This is you
To succeed in this role, we believe you combine scientific credibility with commercial awareness and strong leadership capabilities. You have a cross-functional mindset and understand how areas beyond your immediate regulatory scope, such as CMC and non-clinical development, connect to and influence the overall development and regulatory strategy.
You also are:
Curious, proactive and driven by continuous improvement
Why Join PharmaRelations?
At PharmaRelations, you will have the opportunity to:
Your application
If you have a strong background in Regulatory Affairs and drug development and if you are excited by the opportunity to combine your expertise with client engagement, leadership and business development, we are very interested in hearing from you. Please click Apply to submit your application. For further information about the role and the recruitment process, please contact Kristina Edholm at PharmaRelations (kristina.edholm@pharmarelations.se).
