7 дней назад
Clinical Scientist Director, Early Development Oncology
10 582 245 - 14 317 155€
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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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