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2 дня назад

Scientific Director I (Oncology Early Development)

160 500 - 305 000$
Формат работы
onsite
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
Scientific Director I (Oncology Early Development) (Clinical Development/Oncology): Overseeing clinical trials and research programs in hematology, solid tumors, or cell therapy with an accent on study integrity, medical monitoring, regulatory compliance, and scientific data interpretation. Focus on designing clinical development plans, interpreting safety and efficacy data, and coordinating cross-functional global teams and clinical partners.

Location: South San Francisco, California, United States

Salary: $160,500–$305,000 USD per year

Company

hirify.global develops medicines and solutions for serious health conditions, with key therapeutic areas including immunology, oncology, neuroscience, and aesthetics.

What you will do

  • Lead the direction, planning, execution, and interpretation of clinical trials and research activities in hematology, solid tumors, or cell therapy.
  • Oversee one to two clinical studies, including study integrity, medical monitoring, safety and efficacy data review, and communication of findings.
  • Develop and interpret protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions, and other program documents.
  • Manage enrollment oversight, study timelines, CROs, vendors, and project-related education for investigators and study personnel.
  • Build cross-functional Clinical Development Plans and contribute to translational strategies, due diligence, and business development activities.
  • Ensure compliance with Good Clinical Practices, pharmacovigilance standards, regulatory requirements, and internal quality procedures.

Requirements

  • Bachelor’s degree in a scientific discipline; an MS, PhD, or PharmD is preferred.
  • At least five years of clinical trial experience in the pharmaceutical industry, academia, or an equivalent setting.
  • Knowledge of clinical trial methodology, regulatory and compliance requirements, clinical strategy, and study protocol design.
  • Ability to oversee clinical research programs of moderate complexity with minimal supervision.
  • Ability to collaborate effectively across global, cross-functional teams and support scientific and business strategy.
  • Excellent written and spoken English communication skills required.

Culture & Benefits

  • Paid vacation, holidays, and sick leave.
  • Medical, dental, and vision insurance for eligible employees.
  • 401(k) benefits for eligible employees.
  • Eligibility to participate in long-term incentive programs.
  • Equal opportunity employment environment focused on integrity, innovation, and community impact.

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