Job Summary
A company is looking for a Sr. Biostatistician to contribute statistical expertise to clinical trials and development plans.
Key Responsibilities
- Design and analyze clinical trials and development plans for compounds/programs
- Collaborate with program partners and stakeholders to deliver statistical deliverables for clinical trials
- Ensure compliance with company guidelines and regulatory requirements in statistical processes
Required Qualifications
- Master's or Ph.D. in Statistics or related field with a minimum of 5 years of experience
- Expertise in drug development and advanced knowledge of biostatistics
- Proficiency in statistical software (SAS and/or R)
- Experience in planning and supervising statistical processes for multiple clinical trials
- Ability to work autonomously and collaboratively in a cross-disciplinary team
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