Head of Medical Affairs Poland

• Multiple locations
• Remote

Job Description

Take part in a journey committed to innovation and improving lives

Nordberg Medical is a Swedish biotech company working at the forefront of biomaterial science to reverse functionality loss. With state-of-the-art biomaterials we produce and market innovative medical products that target structural imbalances associated with aging.

In 2021 we passed a critical milestone by receiving CE certification for our first product. JULÄINE of Sweden is a biostimulator that activates natural collagen production in the skin. This positions the company well to pursue an ambitious growth strategy in the aesthetic dermatology market.

Backed by leading investors and extensive R&D we are expanding across multiple therapeutic areas and geographies.

Join an international team of highly talented individuals where your contribution counts. We promote a culture of entrepreneurship multiculturalism and flexibility in more than ten countries. At Nordberg Medical you will have the opportunity to grow and learn to be creative and to contribute to both our product and company success.

Our Medical Affairs team in Europe is growing and we are looking for our new

Head of Medical Affairs Poland

As our Head of Medical Affairs (HMA) Poland you will report into our VP Medical Affairs you will be pivotal in establishing strategic and tactical Medical Affairs leadership in your region. Youll work closely with KOLs physicians and healthcare professionals (HCPs) to lead scientific discussions support trial enrollment and deliver educational programs and training. Serving as the primary medical point of contact your scientific expertise will be instrumental in enhancing team capabilities and customer interactions.

You will mostly work on:

• Reviewing scientific literature to inform company strategy consolidating actionable medical insights.
• Developing regional medical affairs goals translating them into tactics for optimal scientific exchange.
• Managing Key Opinion Leader (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 Maintain knowledge of regulatory guidelines and assist in resolving regulatory issues.
• Ensuring compliance with local regulations and review promotional materials.