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Role Responsibilities:
- Monitor and own the progress of clinical studies at investigative sites.
- Ensure studies are conducted per protocol, SOPs, ICH-GCP, and regulations.
- Coordinate study setup activities like investigator selection and regulatory submissions.
Qualifications:
- Graduate or postgraduate degree in a scientific or healthcare discipline.
- 2.5+ years as a CRA in a CRO or pharma/biotech.
- Fluency in English and local language; domestic travel up to 50-60%.
Culture and Growth:
- Focus on 1-2 studies to become a protocol expert.
- Reasonable travel supports work/life balance.
- Voice is heard in a smaller CRO with direct line management support.
Compensation and Benefits:
- Salary range 173,000-259,400 PLN gross per annum.
- Eligible for discretionary annual bonus, private medical insurance, MultiSport Card, life insurance, pension, home working allowance, and vacation.
Precision For Medicine
Precision for Medicine, Oncology & Rare Disease is a precision medicine CRO that combines novel clinical trial designs, operational expertise, and biomarker analytics to advance oncology and rare disease treatments. The company fosters a culture with high CRA retention, small team influence, and a focus on work/life balance.