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Edison Scientific via Ashby

Clinical Operations SME

Level not stated United States
still open verified 1d ago posted 4d ago checked just now
Apply at jobs.ashbyhq.com

This is the employer's own posting, not a copy on a job board.

What we know

Is it still open?

Confirmed still open

Last checked 1d ago — checked against the employer's own applicant tracking system, which is the company answering directly.

We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.

Check this listing's status as JSON

How old is it?

Posted 4d ago

The date the source published, not the day we noticed it (2026-09-10). Last seen at its source just now.

Is it remote?

Remote available (U.S. Only)

That is the location the employer filed this posting under. Quoted as written — we do not re-word the source's own location.

Who may apply?

United States

The description states no restriction of its own. This is the source's own tag.

Pay not stated

Similar roles pay $117.5k–130k/yr

Middle 50% of 713 listings that do state pay — Healthcare · all levels · United States · USD/year. This employer has published no salary; this is what comparable listings we hold disclose, never converted between currencies or periods. How this is calculated.

Skills named in the ad

Data AnalysisGCPPythonUser Stories

Recognised terms only, from a fixed vocabulary — this is what CV matching compares against.

Carried by 1 source

The listing

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 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

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.

Apply at jobs.ashbyhq.com