Forward-Deployed Clinical Operations Subject Matter Expert

We're looking for a Forward-Deployed Clinical Operations Subject Matter Expert to join our Forward Deployed team, working onsite with pharma and biotech partners alongside our engineers. Your job: ensure our AI agents produce clinical trial outputs that are operationally sound, protocol ready, and aligned with how clinical teams actually run studies.

You'll evaluate agent performance on clinical trial design tasks, work with our partners' clinical operations and development teams to identify where AI can streamline their workflows, and bring real-world trial execution knowledge to everything our platform generates. You're the person who knows whether an AI drafted protocol section or study design would hold up to regulatory standards.

This is embedded, partner-facing work. You'll build relationships with clinical leaders, understand their operational constraints and regulatory requirements, and feed that knowledge back to our AI team to improve how our platform reasons about trial design, feasibility, and execution.

This position would ideally sit out of Boston, NYC, or San Francisco; but also flexible for fully remote with 20-40% travel.

Responsibilities

Evaluate and improve AI agent performance on clinical operations tasks including protocol development, study design, site feasibility, patient enrollment strategy, and clinical data analysis

Design benchmarks and acceptance criteria for clinical trial-focused agent workflows

Partner with clinical operations and development teams at client organizations to integrate AI agents into their trial planning and execution workflows

Serve as the clinical operations authority on AI-generated outputs, assessing operational feasibility, GCP compliance, and alignment with real-world trial execution

Collaborate daily with Forward Deployed Engineers and Computational Biologists on each account

Support engagement scoping, success metrics, and technical evaluation with GTM

Requirements

5+ years of experience in clinical operations or clinical development within the pharmaceutical or biotechnology industry, ideally within a sponsor organization

Bachelor's degree required; advanced degree preferred

Experience designing Phase I through III clinical trials with strong expertise in study design and protocol development

Experience in oncology, immuno-oncology, immunology, cardiovascular, neurology, or hepatology (MASH) therapeutic areas

Experience analyzing clinical trial data and translating findings into operational decisions

Strong knowledge of GCP guidelines and regulatory requirements for clinical trial conduct

Familiarity with the end-to-end trial lifecycle from startup through closeout

Ability to travel domestically 20-40% of the time

Nice to Have

Medical monitoring or Study Management experience

Familiarity with clinical trial management systems (CTMS), EDC platforms, or trial analytics tools

Python proficiency

High comfort with ambiguity and fast iteration