Lead or contribute to design, analysis, and interpretation of clinical studies.
Collaborate with sponsor, PM, clinical team, data managers, and statist programmers.
Oversight of contracted statistical output and activities across studies.
Provide statistical input to protocols, SAPs, data reviews, and study reports.
Mentor junior statisticians and represent statistics in internal/external meetings.

🎯 Requirements

Master’s degree or higher in biostatistics or related field.
Experience in contract research organization environments.
Strong communication and presentation skills.
Proficiency in statistical programming (SAS preferred).
Cross-functional collaboration; knowledge of ICH/regulatory landscape.
Fluency in English; knowledge of advanced statistical methods (survival, logistic, mixed models).

🎁 Benefits

Remote-friendly with global team.
Collaborative international culture.
Opportunity to work on rare disease and oncology trials.

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