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2 дня назад

Forward-Deployed Clinical Operations Subject Matter Expert (AI)

180 000 - 250 000$
Формат работы
remote (только USA)/onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Forward-Deployed Clinical Operations Subject Matter Expert (AI): Evaluating and improving AI agents for clinical trial design, protocol development, site feasibility, enrollment strategy, and clinical data analysis with an accent on operational feasibility, GCP compliance, and real-world trial execution. Focus on designing workflow benchmarks, integrating AI agents into pharma and biotech trial processes, and translating clinical operations expertise into reliable, regulatory-ready outputs.

Location: Remote within the U.S.; ideally based in Boston, New York City, or San Francisco, with 20–40% domestic travel and onsite work with pharma and biotech partners

Salary: $180,000–$250,000 annually, plus equity

Company

hirify.global Scientific builds and deploys AI scientist agents to accelerate scientific research and the development of new medicines.

What you will do

  • Evaluate and improve AI agent performance across protocol development, study design, site feasibility, patient enrollment strategy, and clinical data analysis.
  • Design benchmarks and acceptance criteria for clinical-trial agent workflows.
  • Partner with clinical operations and development teams to integrate AI agents into trial planning and execution.
  • Assess AI-generated outputs for operational feasibility, GCP compliance, regulatory alignment, and real-world trial execution.
  • Collaborate with Forward-Deployed Engineers and Computational Biologists on partner accounts.
  • Support engagement scoping, success metrics, and technical evaluations with go-to-market teams.

Requirements

  • 5+ years of experience in clinical operations or clinical development within the pharmaceutical or biotechnology industry.
  • Bachelor’s degree required; an advanced degree is preferred.
  • Experience designing Phase I–III clinical trials, including study design and protocol development.
  • Experience in oncology, immuno-oncology, immunology, cardiovascular, neurology, or hepatology/MASH.
  • Experience analyzing clinical trial data and translating findings into operational decisions.
  • Strong knowledge of GCP guidelines, regulatory requirements, and the full trial lifecycle from startup through closeout.

Nice to have

  • Medical monitoring or study management experience.
  • Familiarity with CTMS, EDC platforms, or trial analytics tools.
  • Python proficiency.
  • Comfort with ambiguity and fast iteration.

Culture & Benefits

  • Mission-driven, fast-moving environment with close collaboration across science and engineering disciplines.
  • Full healthcare coverage, including 100% employer-paid premiums for employees and dependents.
  • Paid parental leave, fertility coverage, new-parent support, and mental health services.
  • 401(k) matching, commuter benefits, quarterly health and wellness benefits, and pet-care support.
  • Daily office lunches, late-work dinners, team off-sites, and company events.

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