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1 день назад

Clinical Development Director, Early Development Oncology

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
Clinical Development Director, Early Development Oncology (Clinical Research/Drug Development): Leading early-phase clinical development of oncology compounds from first-in-human studies through proof-of-concept with an accent on clinical strategy, trial design, biomarker use, and safety and efficacy evaluation. Focus on developing protocols and regulatory submissions, interpreting pharmacodynamic and pharmacokinetic data, and guiding cross-functional and external oncology collaborations.

Location: Washington D.C., District of Columbia, United States

Company

hirify.global is a biotechnology company developing medicines for serious diseases across oncology, inflammation, general medicine, and rare disease.

What you will do

  • Lead early-phase clinical development of oncology compounds from first-in-human studies through proof-of-concept.
  • Design and implement clinical development strategies for oncology therapeutic candidates.
  • Prepare clinical development plans, protocols, informed consents, Investigator Brochures, and regulatory submissions.
  • Review clinical safety, efficacy, pharmacodynamic, and pharmacokinetic data.
  • Develop and apply clinical biomarker strategies to support drug development.
  • Collaborate with precision medicine, research, late development, regulatory, safety, commercial, and external oncology partners.

Requirements

  • MD or DO degree from an accredited medical school.
  • At least 2 years of industry or academic clinical research or drug development experience.
  • Experience designing, monitoring, and implementing clinical trials and interpreting trial results.
  • Experience with early-stage clinical trials, pharmaceutical sponsors, or clinical trial methodology.
  • Leadership, collaboration, decision-making, and alignment-building skills in a matrix environment.
  • Strong interpersonal and presentation skills, including communication with internal stakeholders and external collaborators.

Nice to have

  • Board certification or eligibility in oncology.
  • Oncology residency training and relevant subspecialty experience.
  • Basic research experience and a publication track record.
  • Three or more years of relevant drug development experience in pharmaceutical industry or academia.

Culture & Benefits

  • Collaborative, innovative, and science-based working environment.
  • Comprehensive medical, dental, vision, life, disability, and flexible spending benefits.
  • Retirement and savings plan with company contributions.
  • Annual bonus program and stock-based long-term incentives.
  • Paid time-off plans and career development opportunities.
  • Flexible work models where applicable to the role.

Hiring process

  • Applications remain open until a sufficient number of applications are received or a candidate is selected.
  • Sponsorship for the role is not guaranteed.

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