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Clinical Trial Design
Data Quality
Role and Responsibilities:
- Lead the design, analysis, and interpretation of clinical studies as study lead for complex trials.
- Oversee statistical activities including protocol development, analysis plans, and data review.
Qualifications:
- Master's degree in biostatistics or related field with strong CRO experience.
- Proficiency in SAS and knowledge of advanced statistical methods and ICH guidelines.
Additional Information:
- Collaborative, international team with work-life balance and flexibility.
- Work on meaningful rare disease and oncology trials with a patient-focused culture.
Ergomed
Ergomed is a specialist clinical research organization focused on rare disease and select oncology indications. With a global team across five continents, they value teamwork, flexibility, and work-life balance.