Clinical Operations Subject-Matter-Expert
Edison Scientific · United States · $180,000–$250,000 (stated in the posting)
About Us
Edison Scientific builds and deploys AI scientist agents to accelerate science and the development of new medicines. We are an ambitious team run by scientists and engineers from leading institutions across biology, physics, chemistry, and AI.
Role
We're looking for a 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.
Key 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
Required Qualifications
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
Preferred Qualifications
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
Salary
$180k - $250k • Offers equity
Why join us?
We're a fast-moving, mission-driven culture where smart people do their best work and actually enjoy doing it. We also offer full-time employees the following:
Competitive salary and equity
Full healthcare coverage; we pay 100% of premiums for you and your dependents
Support for growing families, including a yearly new parent stipend and fertility coverage through Carrot
Mental health support through Rula, our in-network therapist and psychiatrist network with fast availability
12 weeks of paid parental leave for maternity, paternity, and adoption
Pet care support with a yearly employer-funded stipend for your animal companions
Commuter benefits so you can pay for transit and parking with pre-tax dollars
401(k) company matching
$300 health and wellness benefit quarterly
Lunch is on us every day you're in the office, and dinner is on us when you're working late
Regular team off-sites and company events
Edison Scientific is an equal opportunity employer. We do not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other protected characteristic under applicable law.