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Associate Scientific Director (Oncology Early Development)

141 500 - 268 500$
Тип работы
fulltime
Грейд
director
Английский
c1
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
Associate Scientific Director (Oncology Early Development) (Clinical Development/Oncology): Overseeing the planning, execution, interpretation, and reporting of Phase 1 clinical trials supporting oncology product development with an accent on protocol design, safety and efficacy data, regulatory compliance, and cross-functional collaboration. Focus on designing first-in-human studies, interpreting accumulating clinical data, preparing regulatory and scientific documents, and ensuring adherence to Good Clinical Practices and pharmacovigilance standards.

Location: North Chicago, Illinois, or South San Francisco, California, United States

Salary: $141,500–$268,500 per year

Company

hirify.global discovers and delivers medicines and solutions for serious health issues, with key therapeutic areas including immunology, oncology, neuroscience, and aesthetics.

What you will do

  • Oversee the planning, design, execution, and interpretation of clinical trials and research activities within an oncology clinical development program.
  • Manage the design and implementation of first-in-human Phase 1 study protocols and coordinate education for investigators, site personnel, and study staff.
  • Review, interpret, and communicate accumulating safety and efficacy data while supporting enrollment oversight and key study timelines.
  • Contribute to protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions, responses, and Clinical Development Plans.
  • Collaborate with Discovery, Medical Affairs, Commercial, Clinical Operations, and other cross-functional teams.
  • Support opinion leader interactions and maintain compliance with clinical, regulatory, quality, and pharmacovigilance standards.

Requirements

  • Bachelor’s degree in a scientific discipline and an advanced degree such as an MS or PhD.
  • Clinical trial experience in the pharmaceutical industry, academia, or an equivalent setting.
  • Ability to provide input and direction to clinical research under appropriate supervision.
  • Knowledge of clinical trial methodology, regulatory and compliance requirements, and study protocol design.
  • Strong collaboration skills in cross-functional environments and ability to support global scientific and business strategy.
  • Excellent oral and written English communication skills required.

Culture & Benefits

  • Cross-functional collaboration across clinical, scientific, medical, commercial, and discovery teams.
  • Opportunities to build therapeutic-area expertise through conferences, medical literature, and training.
  • Paid time off, including vacation, holidays, and sick leave.
  • Medical, dental, and vision insurance for eligible employees.
  • 401(k) and eligibility to participate in long-term incentive programs.

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