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4 дня назад

Clinical Scientist Director, Early Development Oncology

13 116 690 - 17 746 110€
Формат работы
remote (только Spain)
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
Spain
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, clinical trial quality, and regulatory compliance. Focus on designing and monitoring oncology trials, identifying clinical data risks, coordinating cross-functional collaborators and CROs, and supporting regulatory submissions and study readouts.

Location: Spain — Remote

Salary: €131,166.90–€177,461.10 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

  • Support early-phase oncology clinical development by translating scientific and clinical strategy into study concepts, protocols, and execution plans.
  • Provide clinical and scientific expertise for assigned therapeutic areas and indications, with responsibility for protocol execution and data integrity.
  • Contribute to medical monitoring, subject-level clinical data review, data quality assessments, and identification of trends, risks, and emerging issues.
  • Review and interpret clinical trial data for accuracy, completeness, protocol adherence, and regulatory compliance.
  • Coordinate with cross-functional teams, collaborators, consultants, and CROs to deliver clinical trials and obtain governance approval.
  • Support study data readouts, clinical regulatory responses, scientific publications, and conference presentations.

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 at least 5 years.
  • Industry or academic experience in early-phase oncology drug development.
  • 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.
  • Strong written, verbal, communication, and presentation skills for engaging leadership committees and external stakeholders.

Nice to have

  • Experience improving clinical trial processes.
  • Experience drafting regulatory submission documents and authoring responses for health authority interactions.
  • 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 environment.
  • Comprehensive employee benefits, including medical, dental, vision, life, and disability coverage.
  • Retirement and savings plans, flexible spending accounts, and stock-based long-term incentives.
  • Discretionary annual bonus program and award-winning time-off plans.
  • Flexible work models, including remote and hybrid arrangements where possible.
  • Career development opportunities and support for professional and personal well-being.

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