Senior Director, Medical Monitor – Respiratory Indications

🔥 0 minutes ago

🇺🇸 United States – Remote

💵 $277k - $400k / year

⏰ Full Time

🟠 Senior

👨‍⚕️ Medical Director

🦅 H1B Visa Sponsor

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Logo of Generate Biomedicines

Generate Biomedicines

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.

📋 Description

• Provide day-to day medical oversight for late-stage clinical trials in asthma and/or COPD ensuring patient safety, protocol compliance, data integrity and inspection readiness • Serve as primary medical contact for clinical sites, investigators, and CROs Perform subject eligibility review, ongoing data reviews, manage study queries, identify and assess protocol deviations • Serve as a member of the Clinical Development, Safety Management and Study Execution teams • Contributing author and key reviewer of core clinical and regulatory documents including IB, ICF, RFI, study protocols, DSUR • Support study oversight committees including DSMB, endpoint adjudication committee, etc.Collaborate cross-functionally with Clinical Operations, Regulatory, Biostatistics, and Pharmacovigilance • Interpret clinical trial data and contribute to study reports, regulatory filings, and publications

🎯 Requirements

• MD (required); board certification in Pulmonology or Allergy & Immunology preferred • 8+ years of clinical development experience in the biopharma industry • Extensive expertise in asthma and respiratory clinical trial design, oversight, and execution • Strong cross-functional leadership and communication skills • Proven ability to collaborate with internal teams and external stakeholders.

🏖️ Benefits

• annual bonus • equity compensation • competitive benefits package

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