9 дней назад
Clinical Scientist Director - Late Development Oncology (Oncology)
52 313 930 - 70 777 670PLN
Мэтч & Сопровод
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Описание вакансии
Текст:
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
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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