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4 дня назад

Director, Clinical Science (Clinical Trials)

234 190 - 287 980$
Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
director
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
Director, Clinical Science (Clinical Trials): Overseeing clinical aspects of multiple early-phase oncology trials, including protocol authoring, medical monitoring, clinical data review, site interactions, and clinical presentations with an accent on study execution, data quality, and cross-functional collaboration. Focus on managing complex Phase 1–2 studies, identifying data trends and inconsistencies, resolving queries, and coordinating clinical deliverables across investigative sites and supporting functions.

Location: Fully remote within the United States, with occasional travel for collaboration, team events, meetings, or other business needs. Salary bands vary by New York City, Boston, San Francisco Bay Area, Salt Lake City, and other U.S. locations.

Salary: $234,190–$287,980 in New York City, Boston, and the San Francisco Bay Area; $212,900–$261,800 in Salt Lake City and other U.S. locations. Eligible for an annual bonus, equity compensation, and comprehensive benefits.

Company

hirify.global is a clinical-stage TechBio company using an AI-native platform, automated biology, chemistry, and multimodal data to develop investigational medicines.

What you will do

  • Oversee the clinical aspects of multiple early-phase Phase 1–2 clinical studies.
  • Author protocols, amendments, medical monitoring plans, annual reports, study updates, clinical study reports, and other clinical documents.
  • Conduct routine medical monitoring and interact with investigative sites regarding patient eligibility and treatment inquiries.
  • Review clinical data, issue and close queries, review tables, listings, and figures, and identify trends or inconsistencies.
  • Present protocols, study procedures, and clinical data to investigative sites, management, and internal or external audiences.
  • Coordinate cross-functionally with Clinical Operations, Medical Directors, CMC, Data Management, CROs, CRAs, and investigative sites.

Requirements

  • 5–7+ years of experience as a Clinical Scientist in a pharmaceutical or biotech company.
  • Required experience with early-phase Phase 1–2 oncology studies.
  • Strong written and verbal communication and relationship-building skills.
  • Ability to manage multiple complex and competing priorities simultaneously.
  • Ability to operate strategically and tactically and solve issues with a solution-focused approach.
  • Must be located in the United States for this fully remote role.

Nice to have

  • Experience with hematologic malignancies.

Culture & Benefits

  • Fully remote work with occasional business travel.
  • Annual bonus eligibility and equity compensation.
  • Comprehensive benefits package.
  • Values-driven environment emphasizing integrity, ownership, active learning, urgency, and cross-functional collaboration.
  • Opportunity to contribute to clinical development from IND through dose finding, proof of concept, and potentially registration studies.

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