Regulatory Affairs Visionary

21 hours ago


Copenhagen, Copenhagen, Denmark Black Swans Exist Full time

Black Swans Exist, a clinical-stage biotech company revolutionizing microbiome-based therapies for women's reproductive health, seeks a seasoned Director of Regulatory Affairs to spearhead their global regulatory strategies.

About the Role

In this high-impact position, you will drive the development and approval of innovative biologics, combination drug-device products, and companion diagnostics. You'll collaborate closely with cross-functional teams and regulatory authorities, ensuring strategies align with global standards and pave the way for clinical success.

Key Responsibilities:

  1. Develop and execute global regulatory strategies for clinical development, Phase 2, and beyond.
  2. Oversee the preparation, review, and submission of INDs, CTAs, and other regulatory filings.
  3. Lead interactions with EMA and FDA, including scientific advice meetings, Type A/B/C meetings, and more.
  4. Craft and refine regulatory plans for biologics and combination products, considering EU and US requirements.
  5. Provide strategic and tactical guidance on regulatory submissions, study designs, and compliance.
  6. Build and enhance organizational capabilities in Regulatory Affairs, fostering a culture of operational and strategic excellence.

What We're Looking For:

  1. Advanced degree in life sciences, pharmacy, or related fields.
  2. 10+ years of global Regulatory Affairs experience, particularly in biologics and combination products.
  3. Proven success with EMA and FDA submissions, and regulatory strategy development.
  4. Experience navigating complex regulatory landscapes, including CTA or IND approvals.
  5. A strategic mindset with operational agility, especially in biotech or small pharma environments.
  6. Strong leadership, interpersonal, and communication skills, adept at matrix management.


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