4 дня назад
Clinical Scientist Director, Early Development Oncology
52 313 930 - 70 777 670PLN
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, 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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