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7 дней назад

Clinical Scientist Director, Early Development Oncology

10 582 245 - 14 317 155€
Формат работы
onsite
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
Portugal
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 Scientist Director, Early Development Oncology (clinical trials): Supporting early-phase oncology clinical development by translating scientific strategy into protocol execution, medical data review, and clinical data quality with an accent on data integrity, regulatory compliance, and cross-functional delivery. Focus on monitoring subject-level data, identifying trial risks, interpreting results, and designing high-quality clinical plans and study protocols.

Location: Lisbon, Portugal

Salary: €105,822.45–€143,171.55 annually

Company

hirify.global is a biotechnology company researching, manufacturing, and delivering medicines across oncology, inflammation, general medicine, and rare disease.

What you will do

  • Support early-phase oncology clinical development by translating scientific and clinical strategy into study concepts, protocols, and related documents.
  • Act as a clinical and scientific subject-matter expert for assigned therapeutic areas and disease indications.
  • Provide hands-on oversight of protocol execution, medical monitoring, clinical data review, and data quality throughout the trial lifecycle.
  • Identify trends, risks, and emerging issues through subject-level data assessment and data monitoring plans.
  • Collaborate with cross-functional teams, collaborators, consultants, and CROs to deliver clinical trials and maintain protocol integrity.
  • Present scientific information and support interpretation of results, regulatory interactions, publications, and conference presentations.

Requirements

  • Doctorate degree plus 4 years of life sciences or healthcare experience; or master’s degree plus 7 years; or bachelor’s degree plus 9 years.
  • Experience designing, monitoring, and implementing oncology clinical trials in compliance with Good Clinical Practice and regulatory requirements.
  • Experience with clinical data analysis, data cleaning, database lock, data extraction, and production of data outputs.
  • Ability to communicate scientific concepts and clinical data clearly to internal and external leadership committees.
  • Experience drafting regulatory submission documents and clinical regulatory responses.

Nice to have

  • At least 5 years of pharmaceutical clinical drug development experience.
  • Early-phase oncology drug development experience in industry or academia.
  • A proven track record of improving clinical trial processes.
  • Experience with Spotfire or other clinical data analysis tools.

Culture & Benefits

  • Collaborative, innovative, and science-based work environment.
  • Comprehensive health, dental, vision, life, and disability coverage.
  • Retirement and savings plans with company contributions.
  • Annual bonus program and stock-based long-term incentives, subject to eligibility.
  • Paid time off and career development opportunities.
  • Flexible work models, including remote and hybrid arrangements where possible.

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