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4 дня назад

Clinical Scientist Director, Early Development Oncology

52 313 930 - 70 777 670PLN
Формат работы
remote (только Poland)
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
Poland
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 development/oncology): Supporting early-phase oncology clinical development by translating scientific and clinical strategy into protocol execution, medical data review, and decision-ready clinical data with an accent on data integrity, regulatory compliance, and cross-functional trial governance. Focus on monitoring subject-level data, identifying clinical risks, interpreting trial results, and managing protocol and data-quality activities across the trial lifecycle.

Location: Poland — Remote

Salary: 523,139.30–707,776.70 PLN annually

Company

Global biotechnology company developing innovative medicines for serious illnesses 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.
  • Provide clinical and scientific oversight of protocol execution, medical monitoring, clinical data review, and data-quality assessments.
  • Analyze subject-level and trial-level data to identify trends, risks, emerging issues, and protocol or regulatory deviations.
  • Contribute to clinical trial implementation, data interpretation, study readouts, database lock, data extraction, and production of data outputs.
  • Collaborate with cross-functional teams, collaborators, consultants, and CROs to deliver clinical projects and maintain protocol integrity.
  • Present scientific information and actively manage issues across internal and external stakeholders.

Requirements

  • Doctorate degree and 4 years of life sciences or healthcare experience; or master’s degree and 7 years; or bachelor’s degree and 9 years.
  • Experience designing, monitoring, and implementing oncology clinical trials and interpreting results in compliance with Good Clinical Practice and regulatory requirements.
  • Experience in pharmaceutical clinical drug development, preferably including early-phase oncology development.
  • Experience with clinical data analysis tools such as Spotfire or equivalent platforms.
  • Experience drafting regulatory submission documents and clinical regulatory responses.
  • Strong written, oral, communication, and presentation skills for explaining scientific concepts and data to leadership committees.

Nice to have

  • Proven track record of improving clinical trial processes.
  • Experience contributing to scientific publications and presentations at scientific conferences.

Culture & Benefits

  • Collaborative, innovative, and science-based working environment.
  • Comprehensive employee benefits package including medical, dental, vision, life, disability, and flexible spending plans.
  • Retirement and savings plan with company contributions.
  • Discretionary annual bonus program and stock-based long-term incentives.
  • Paid time off and career development opportunities.
  • Flexible work models, including remote and hybrid arrangements where available.

Hiring process

  • Applications remain open until a sufficient number of candidates are received or a candidate is selected.
  • Reasonable accommodation is available during the application and interview process.

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