Nordberg Medical

1 Job

126 Employees

About the Company

Nordberg Medical is a Swedish biotech company driven by purposeful innovation. We specialize in the development, manufacturing and commercialization of advanced medical biomaterials. By bridging nature and technology, we develop next-generation biomaterials that empower the body‘s natural regenerative potential. Driven by science, we challenge standards and transform the field of bio-regeneration – delivering regenerative solutions for aesthetic medicine and beyond.

Listed Jobs

Company Name: Nordberg Medical
Job Title: Studies and Publications Specialist
Job Description: **Job title** Studies and Publications Specialist **Role Summary** Support the Studies and Publications Director in managing clinical studies and case report projects for an aesthetic medical device portfolio. Ensure compliance with protocols, SOPs, and regulatory standards while coordinating timelines, documentation, and communication with Key Opinion Leaders and cross‑functional teams. **Expectations** - Execute clinical study processes (ITT/IIS) and publication cycle from planning through completion. - Maintain accurate study trackers, documentation, and deliverable oversight. - Serve as the main liaison for KOLs and internal departments (Clinical Affairs, R&D, Medical Affairs). - Review manuscripts, abstracts, and case reports; assist in scientific communication materials for congresses and publications. **Key Responsibilities** - Develop and maintain study management procedures and documentation. - Coordinate study timelines, milestones, and quality checks. - Communicate regularly with KOLs, investigators, and internal teams to resolve issues proactively. - Collaborate with Regulatory and Marketing to ensure GCP, ISO 14155/14385, and MDR compliance. - Contribute to manuscript preparation, scientific presentations, and publication strategy. - Attend conferences and group meetings to stay current on industry developments. **Required Skills** - Strong organizational and project management capabilities. - Excellent written and verbal communication in English. - Proficient in clinical study processes and regulatory requirements (GCP, ISO 14155/14385). - Ability to work collaboratively across Clinical, Regulatory, and Marketing departments. - Experience in medical writing or manuscript review preferred. - Multilingual abilities a plus. **Required Education & Certifications** - Bachelor’s or Master’s degree in Life Sciences, Medicine, or related field. - Minimum 3 years of experience in clinical research or medical affairs, ideally within aesthetics or Class IIb/III medical devices.