Associate Director Biostatistician Consultant - Remote in Western EU(24 months contract)
Related skills
r sas biostatistics📋 Description
- Independently design protocols for multiple therapeutic areas
- Draft protocols/amendments and SAPs; perform analyses
- Prepare interim and final reports for regulatory agencies
- Represent Biostatistics in study/team meetings
- Support submission activities with integrated safety/efficacy summaries
- Lead deliverables coordination with statist programmers and data managers
🎯 Requirements
- MS or PhD in Statistics or Biostatistics
- PhD + 6 years (or MS + 11 years) biotech/pharma clinical trial experience
- Phase I–III trials; proficient in SAS; R desirable
- Excellent oral and written communication skills
- Regulatory submissions experience in US/Europe/Japan desirable
🎁 Benefits
- Global CRO with focus on quality and development
- Confident client-facing role with independent work style
- Career development and training opportunities
- Equal opportunity employer and inclusive culture
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