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9 дней назад

Clinical Scientist Director - Late Development Oncology (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 - Late Development Oncology (Oncology): Supporting late-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 collaboration. Focus on monitoring clinical trial data, identifying risks and emerging issues, improving data quality, and guiding protocol governance through final approval.

Location: Poland - Remote

Salary: 523,139.30–707,776.70 PLN annually

Company

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

What you will do

  • Provide clinical and scientific subject-matter expertise for late-phase oncology development.
  • Oversee protocol execution, clinical data review, and data quality throughout the trial lifecycle.
  • Support medical monitoring and identify trends, risks, and emerging issues in subject-level data.
  • Translate clinical strategy into study concepts, protocols, clinical plans, and related documents.
  • Coordinate with cross-functional teams, collaborators, consultants, and CROs to deliver clinical trials.
  • Contribute to clinical data interpretation, regulatory activities, study readouts, and protocol governance.

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 in pharmaceutical clinical drug development, preferably including late-phase oncology studies.
  • 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.
  • Experience drafting regulatory submission documents and clinical regulatory responses.
  • Strong written, oral, communication, presentation, and cross-functional leadership skills.

Nice to have

  • A proven track record of improving clinical trial processes.
  • Experience contributing to scientific publications and presentations at scientific conferences.
  • Experience with Spotfire or other clinical data analysis tools.

Culture & Benefits

  • Collaborative, innovative, and science-based working culture.
  • Comprehensive health, dental, vision, life, disability, and flexible spending benefits.
  • Retirement and savings plan 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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