Lead design, analysis, and interpretation of clinical studies.
Collaborate with sponsor, PM, clinical team, data managers, writers, programmers.
Oversee statistical output and activities across protocols and analysis plans.
Review and input into clinical protocols, SAPs, safety reviews, and reports.
Mentor junior statisticians and provide statistical guidance.
Represent Biostatistics in internal/external meetings and audits.

🎯 Requirements

Master’s or higher in biostatistics or related field.
Experience in CROs and clinical trials.
Strong communication and presentation skills.
Proficiency in SAS; MS Office skills.
Cross-functional collaboration experience.
Knowledge of ICH/regulatory landscape; advanced methods.

🎁 Benefits

Remote work option; global team collaboration.
Opportunity to work on rare disease/oncology trials.
Competitive environment with industry impact.

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