Strategic Medical Affairs Director for Nordic Region

2 days ago

Stockholm, Stockholm, Sweden Nordberg Medical Full time
About Nordberg Medical

Nordberg Medical is a pioneering biotech company that leverages biomaterial science to restore functionality loss. Our cutting-edge biomaterials enable the development and marketing of innovative medical products addressing structural imbalances associated with aging.

Our journey began with a critical milestone, receiving CE certification for our first product, JULÄINE of Sweden. This breakthrough positions us well to pursue an ambitious growth strategy in the aesthetic dermatology market.

We are backed by leading investors and extensive R&D, expanding across multiple therapeutic areas and geographies.

As a member of our international team of highly skilled professionals, your contribution will be valued and fostered in a culture of entrepreneurship, multiculturalism, and flexibility in over ten countries. At Nordberg Medical, you will have opportunities to grow, learn, create, and contribute to both our product and company success.

Job Description

We seek a highly experienced professional to fill the role of Head of Medical Affairs (HMA) Nordics. As HMA Nordics, you will report directly to our VP Medical Affairs and play a pivotal part in establishing strategic and tactical Medical Affairs leadership in your region.

You will work closely with Key Opinion Leaders (KOLs), physicians, and healthcare professionals to lead scientific discussions, support trial enrollment, and deliver educational programs and training. Your scientific expertise will be instrumental in enhancing team capabilities and customer interactions.

Key Responsibilities:
  • Reviewing scientific literature to inform company strategy and consolidating actionable medical insights.
  • Developing regional medical affairs goals and translating them into tactics for optimal scientific exchange.
  • Managing KOL relationships and supporting faculty development activities.
  • Supporting clinical research (ISS and SIS) by identifying investigators, managing protocols, and reviewing study data. Collaborating with regulatory affairs for submissions and product approvals.
  • Maintaining knowledge of regulatory guidelines and assisting in resolving regulatory issues.
  • Ensuring compliance with local regulations and reviewing promotional materials.

This is a collaborative role where you will be part of a cross-functional local team in the Nordics, as well as the global Medical Affairs team. As an early member of the Nordberg Medical team, you'll have a unique opportunity to contribute to our journey as a global leader in regenerative solutions. Regular travel to conferences and group meetings will be required.

Requirements
  • Successful experience in medical affairs, scientific communications, and/or clinical research ideally within aesthetics; we could consider a medical device or pharma industry background.
  • Advanced degree in a relevant scientific field (MD, PhD, PharmD, etc.).
  • Strong understanding of combination product (drug and medical device) development and regulatory processes.
  • Proficiency in both Swedish and English with excellent communication skills.

Initially, you will start as an individual contributor but the role will most likely expand into a people management position with MSLs reporting to you as Nordberg Medical grows its business.

Why Choose Us?
  • Impact: As a key member of our local team, you'll have the chance to shape and strengthen our presence in this vital market.
  • Continuous Development: We commit to fostering your professional growth through ongoing training and development opportunities.
  • Entrepreneurial Environment: Join a global, inclusive team that encourages innovation and creativity, empowering you to make a meaningful impact.
  • Flexible Work Arrangements: We believe a flexible work environment is attainable by building strong relationships based on trust with our employees.

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