Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Обязанности описаны понятно, а работа сочетает клиническую науку и AI, но без информации о зарплате сложно оценить общую привлекательность предложения.
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Зарплата не указанаПонятные задачиAI в медицинеДва офиса
Оценка от Hirify AI
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Medical Writer (AI Healthtech): Producing scientific publications, white papers, value dossiers, conference materials, and medical content for an AI-driven clinical platform with an accent on clinical trial methodology, regulatory considerations, and patient-centric scientific communication. Focus on shaping protocol design support, eligibility logic, endpoint frameworks, and medically sound product workflows while representing the platform with sponsors, KOLs, and regulators.
Location: Hybrid work from the Austin or Barcelona hubs
Company
hirify.global is a Healthtech company using AI to accelerate drug development and improve patient outcomes.
What you will do
Produce peer-reviewed publications, white papers, value dossiers, conference materials, and other scientific deliverables.
Provide medical and scientific input on clinical platform functionalities, including protocol design support, eligibility logic, and endpoint frameworks.
Partner with Product and Commercial teams to align AI models and workflows with standards of care, clinical guidelines, and regulatory considerations.
Translate complex clinical and scientific concepts into clear content for sponsors, KOLs, internal teams, and external publications.
Support advisory boards, scientific conferences, and strategic partner discussions as a scientific representative.
Help shape the platform's medical and therapeutic direction around real-world drug and device development challenges.
Requirements
Advanced scientific or clinical background in life sciences, pharmacy, medicine, or a related field; a medical degree, PharmD, or clinical PhD is required.
Experience in clinical development, medical affairs, medical writing, scientific communications, or a related pharma or biotech function.
Strong understanding of clinical trial methodology, endpoint selection, and benefit-risk assessment.
Excellent scientific writing skills with published or client-facing work.
Strong stakeholder management skills and high integrity.
Nice to have
Experience with digital health and AI-driven platforms.
Exposure to multiple therapeutic areas or indications.
Experience presenting at scientific conferences or serving on advisory boards.
Hands-on experience with protocols, eligibility criteria, endpoints, or regulatory documents.
Culture & Benefits
International, collaborative, and diverse working environment.
Hybrid work model.
Comprehensive private health coverage.
Company events and a pet-friendly office.
MacBook provided for work.
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