Senior Director, Head of Clinical Operations

4 days ago

Stockholm, Sweden Bioarctic Full time

Join BioArctic and help shape the future of neuroscience drug development

We are a pioneering biopharma company focused on innovative treatments for neurodegenerative diseases. We are seeking an experienced Senior Director to lead our Clinical Operations & Medical Science team within Clinical Development and Regulatory Affairs (CDRA).

As Senior Director, Head of Clinical Operations & Medical Science at BioArctic, you will lead and shape our clinical operations and medical science function, making a significant contribution to our mission of developing innovative treatments for neurodegenerative diseases. This is an opportunity to provide scientific and operational leadership across clinical development programmes in a dynamic, cross-functional environment. You will ensure the highest standards in clinical drug development including planning, execution, and oversight of clinical trials. You will play a key part in BioArctic's continued expansion as a world-leading biopharmaceutical company.

Your Impact

In this role, you will:

  • Set strategy and oversee all clinical operations at BioArctic
  • Provide expert input to clinical development plans and operational activities
  • Oversee global clinical trials from planning to close-out, ensuring timelines, budgets, and quality standards
  • Develop and mentor a high-performing team, fostering growth and collaboration
  • Partner with CROs and study centers to deliver excellence in clinical execution
  • Ensure compliance with GCP, ICH guidelines, and regulatory requirements
  • Leading external collaborations

Your Profile

  • MSc in Life Sciences or a medical discipline, PhD is preferrable
  • 10+ years in clinical project/study management within global drug development.
  • 5+ years in leadership roles with direct reports
  • Strong expertise in CNS drug development, in building clinical development programs and global clinical operations
  • Experience of sponsor oversight from planning stage to close-out, including CRO management
  • Experience from preparing documentation for clinical trials as well as associated regulatory documentation
  • Excellent strategic, project management, planning, and communication skills.
  • Fluent in English; Swedish is an advantage
  • Experiences in rare disease trials, knowledge in pharmacovigilance and data management oversight is advantageous

If you're ready to make a real difference for patients with high unmet medical needs, apply today and join our mission.

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