Biotech Regulatory Affairs Lead
6 days ago
About Black Swans Exist
Black Swans Exist is a clinical-stage biotech company revolutionizing microbiome-based therapies for women's reproductive health. We are shaping the future of women's health by developing innovative biologics and combination drug-device products.
The Role
We seek a visionary Director of Regulatory Affairs to lead our global regulatory strategies. As a key member of our team, you will drive the regulatory framework for developing and approving our innovative therapies.
Your Key Responsibilities
- Develop and execute global regulatory strategies for clinical development, Phase 2, and beyond.
- Oversee the preparation, review, and submission of INDs, CTAs, and other regulatory filings.
- Lead interactions with EMA and FDA, including scientific advice meetings, Type A/B/C meetings, and more.
- Craft and refine regulatory plans for biologics and combination products, considering EU and US requirements.
- Provide strategic and tactical guidance on regulatory submissions, study designs, and compliance.
- Build and enhance organizational capabilities in Regulatory Affairs, fostering a culture of operational and strategic excellence.
What We're Looking For
- Advanced degree in life sciences, pharmacy, or related fields.
- 10+ years of global Regulatory Affairs experience, particularly in biologics and combination products.
- Proven success with EMA and FDA submissions, and regulatory strategy development.
- Experience navigating complex regulatory landscapes, including CTA or IND approvals.
- A strategic mindset with operational agility, especially in biotech or small pharma environments.
- Strong leadership, interpersonal, and communication skills, adept at matrix management.
Why This Opportunity Matters
- Shape regulatory pathways for cutting-edge treatments.
- Engage directly with regulatory agencies to drive impactful decisions.
- Expand your career as the organization grows, taking on more projects and leadership opportunities.
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