Associate Director, Biostatistics

This is a fully remote position, open to applicants in Spain.

📋 Description

• Serve as the lead statistician for individual studies, related studies, and integrated summaries.

• Design and report on Phase I to IV clinical studies and regulatory submissions, under the guidance of a senior statistician.

• Oversee all statistical components of study design, analysis, validation, and documentation.

• Deliver timely and scientifically robust statistical expertise to clinical development initiatives.

• Create and implement statistical strategies, designs, and analyses for clinical trials.

• Collaborate with teams in clinical development, pharmacology, pharmacovigilance, clinical drug supply, project management, regulatory affairs, medical writing, clinical data management, and clinical operations.

⛳️ Requirements

• MS or MPH in statistics, mathematics, or a related field with a statistical emphasis, along with over 7 years of experience in the pharmaceutical or biotechnology sector.

• PhD in statistics, mathematics, or a related field with a statistical focus, accompanied by more than 2 years of experience in the pharmaceutical or biotechnology industry.

• Familiarity with drug development regulations relevant to statistical analysis.

• Preference for knowledge in the oncology or hematology therapeutic areas.

• Experience with Bayesian and adaptive design is preferred.

• Strong proficiency in SAS and R programming, along with a solid understanding of CDISC models and standards.

• Exceptional writing and communication abilities.

• Proven leadership skills and excellent interpersonal capabilities.

🏝️ Benefits

• Competitive salary and performance-based bonuses.

• Comprehensive health, dental, and vision insurance.

• Generous paid time off and holiday schedule.

• Opportunities for professional development and continuous learning.

• Collaborative and innovative work environment.