4 дня назад
Clinical Scientist Director, Early Development Oncology
13 116 690 - 17 746 110€
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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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