Darum lohnt es sich
Requirements:
• PhD in Statistics/Biostatistics with 5+ years of experience or Master’s with 10+ years.
• Strong knowledge of clinical development and statistical analysis principles.
• Proficiency in SAS and R; experience with NDA/BLA submissions preferred.
• Remote/hybrid work flexibility and global exposure across clinical programs.
• Opportunities for professional growth, learning, and technical capability building.
• Competitive salary, healthcare, paid leave, and retirement benefits. • Serve as study biostatistician across development programs, authoring Statistical Analysis Plans and overseeing TFL generation.
• Plan and implement statistical analyses for clinical study reports and regulatory submissions.
• Contribute to innovative trial designs, simulations, and process improvements.
Partner Company
The partner company specializes in global clinical development, supporting registration-directed clinical trials across therapeutic areas. It fosters a collaborative, results-oriented culture with a focus on innovation, professional growth, and high-quality deliverables.
