Principal Biostatistician

📋 Description

• Lead or contribute to design, analysis, and interpretation of clinical studies.
• Collaborate with sponsor, PM, clinical team, data managers, medical writers, and programmers.
• Oversee contracted statistical output and activities (protocol sections, SAP, data/safety reviews
• Maintain and review content relevant to trials and provide statistical input to summaries.
• Act as study lead for multiple studies or programs; ensure timelines and quality standards.
• Mentor junior statisticians and represent biostatistics in internal/external meetings and bid

🎯 Requirements

• Master’s degree (or higher) in biostatistics, statistics, mathematics, or related field.
• Strong experience in a Contract Research Organization.
• Communication and presentation skills; proficiency in MS Office.
• Proficiency in SAS (preferred) and collaboration across cross-functional teams.
• Good understanding of ICH/regulatory landscape and advanced methods (survival analysis, logistic
• Fluency in English.

🎁 Benefits

• Collaborative, international team with focus on rare diseases and oncology.
• Opportunities to contribute to product development and regulatory submissions.
• Remote/Hybrid work options and emphasis on work-life balance.