
201 - 500 employees
Founded 2020
🧬 Biotechnology
🤖 Artificial Intelligence
💊 Pharmaceuticals
💰 $370M Series B on 2021-11
Biotechnology • Artificial Intelligence • Pharmaceuticals
Generate Biomedicines is a pioneering therapeutics company that stands at the intersection of machine learning, biological engineering, and medicine. They are leading the development of generative biology, a groundbreaking approach that uses artificial intelligence to create novel medicines with specific therapeutic functions. By studying millions of proteins, Generate Biomedicines has discovered generalizable rules by which nature encodes function, enabling them to generate medicines on demand across multiple therapeutic modalities. Their innovative platform promises to fundamentally change the way medicines are made, expanding technical possibilities and improving speed and success rates in drug discovery.
🕒 3 days ago
🍂 Massachusetts – Remote
💵 $186k - $270k / year
⏰ Full Time
🔴 Lead
👨⚕️ Medical Director
🦅 H1B Visa Sponsor
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201 - 500 employees
Founded 2020
🧬 Biotechnology
🤖 Artificial Intelligence
💊 Pharmaceuticals
💰 $370M Series B on 2021-11
Biotechnology • Artificial Intelligence • Pharmaceuticals
Generate Biomedicines is a pioneering therapeutics company that stands at the intersection of machine learning, biological engineering, and medicine. They are leading the development of generative biology, a groundbreaking approach that uses artificial intelligence to create novel medicines with specific therapeutic functions. By studying millions of proteins, Generate Biomedicines has discovered generalizable rules by which nature encodes function, enabling them to generate medicines on demand across multiple therapeutic modalities. Their innovative platform promises to fundamentally change the way medicines are made, expanding technical possibilities and improving speed and success rates in drug discovery.
• Serve as clinical science lead and core member of clinical development team for respiratory studies • Support day-to-day study execution, ensuring alignment with protocol, timelines, and regulatory requirements • Act as a key scientific contributor to late-stage protocols and regulatory submissions • Participate in medical monitoring activities • Collaborate with Clinical Operations, Regulatory, Biostatistics, Data Management, and Safety teams • Ensure inspection readiness
• Advanced degree (PhD, PharmD, MD, MS, PMP) and 9+ years of industry experience in clinical development • Strong knowledge of clinical research methodologies, regulatory guidelines, and GCP • Demonstrated ability to lead clinical science strategy and execution in late-stage trials • Excellent analytical, communication, and cross-functional collaboration skills • Prior experience authoring clinical protocols, CSRs, and regulatory documents
• Annual bonus • Equity compensation • Competitive benefits package
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