Associate Director, US Clinical Trial Liaison

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November 18

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Generate Biomedicines

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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.

201 - 500 employees

Founded 2020

🧬 Biotechnology

🤖 Artificial Intelligence

💊 Pharmaceuticals

💰 $370M Series B on 2021-11

📋 Description

• Serve as the primary sponsor contact for U.S. clinical trial sites, ensuring consistent communication and support throughout study execution. • Train site personnel on protocols, study objectives, and the scientific rationale for investigational products. • Collaborate with sites to develop and refine patient recruitment strategies to meet enrollment targets. • Identify and resolve operational and compliance challenges in partnership with Clinical Operations and CROs. • Conduct regular monitoring visits (remote and in-person) to build and sustain productive site relationships. • Capture and relay insights from sites to inform operational decisions and protocol optimization. • Contribute to feasibility assessments and site selection activities based on local treatment practices. • Mentor junior CTLs on core responsibilities, compliance expectations, and communication best practices. • Support the implementation of consistent standards across U.S. trial sites

🎯 Requirements

• Bachelor’s degree in a scientific or health-related field required. • 8 years of clinical trial experience in the pharmaceutical or biotech industry, with deep knowledge of clinical operations and trial conduct. • Proven ability to collaborate with investigators, site staff, and clinical operations teams to drive enrollment and ensure study integrity. • Working knowledge of GCP, ICH guidelines, and U.S. regulatory requirements. • Ability to travel up to 60% for site engagement, meetings, and events. • Strong communication, problem-solving, and relationship-building skills. • Comfortable using clinical trial systems (e.g., IRT, EDC, eTMF).

🏖️ Benefits

• annual bonus • equity compensation • competitive benefits package