Lead or contribute to design, analysis, and interpretation of clinical studies
Collaborate with sponsor, PM, clinical team, data managers, writers, and programmers
Oversee statistical output, SAPs, summaries, and study reports
Mentor junior statisticians; provide guidance on complex outputs
Coordinate analyses for IND/NDA/BLA submissions and other filings
Stay current with industry best practices in clinical trial statistics

🎯 Requirements

Master’s degree or higher in biostatistics or related field
Experience in a Contract Research Organization
Strong communication and presentation skills
Proficiency in SAS; MS Office skills
Knowledge of ICH/regulatory landscape and advanced stats methods
Fluency in English

🎁 Benefits

Collaborative, international team across multiple regions
Focus on rare disease and oncology trials
Remote work with European locations flexibility
Opportunity for professional development and leadership exposure

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