Назад
Company hidden
2 дня назад

Clinical Director, Oncology Clinical Development (Medtech)

221 600 - 277 000$
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
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/

TL;DR

Clinical Director, Oncology Clinical Development (Medtech): Leading medical and scientific strategies for hirify.global-sponsored oncology clinical trials focused on minimal residual disease (MRD) with an accent on biomarker-driven interventional and randomized studies. Focus on designing protocols, overseeing patient safety as a Medical Monitor, and driving precision oncology strategies to support regulatory objectives.

Location: Remote (Must be based in the USA)

Salary: $221,600 – $277,000 USD

Company

hirify.global is a global leader in cell-free DNA (cfDNA) testing, specializing in oncology, women's health, and organ health diagnostics.

What you will do

  • Serve as the program-level medical lead for MRD clinical trials, ensuring clinical outcomes, data integrity, and patient safety.
  • Define clinical development strategies and design protocols aligned with regulatory and scientific objectives.
  • Act as Medical Monitor for safety signal detection, adverse event review, and risk mitigation in compliance with GCP.
  • Partner cross-functionally with Clinical Science, Operations, Data Management, and Biostatistics to ensure study execution.
  • Represent the company in interactions with investigators, KOLs, IRBs, and regulatory authorities.
  • Lead the authorship of clinical study reports, manuscripts, abstracts, and conference presentations.

Requirements

  • MD or equivalent degree.
  • Minimum 3 years of industry experience in oncology clinical development.
  • Proven experience serving as Medical Monitor or clinical lead for Phase II–III studies.
  • Strong working knowledge of GCP, ICH guidelines, and regulatory expectations for interventional trials.
  • Must be based in the USA.

Nice to have

  • Board certification in Medical Oncology or Hematology/Oncology.
  • Experience with biomarker-driven development or molecular diagnostics.
  • Prior involvement in FDA meetings and briefing documents.
  • Experience working within matrixed clinical development organizations.

Culture & Benefits

  • Comprehensive medical, dental, vision, life, and disability plans for employees and dependents.
  • 401k and commuter benefits.
  • Free genetic testing for employees and immediate families, including fertility care.
  • Pregnancy and baby bonding leave.
  • Collaborative environment focused on transforming cancer care through precision oncology.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →