Offer summary
Qualifications:
Master or Ph.D. in Statistics or related field, Minimum 6 years of relevant experience, Expertise in drug development within a regulatory environment, Proficiency in statistical software (SAS and/or R), Experience in clinical trial design.
Key responsabilities:
- Lead statistical analysis for clinical development projects
- Collaborate with cross-functional teams for timely deliverables
- Plan, implement and monitor statistical processes for trials
- Communicate complex statistical concepts clearly
- Embrace excellence and innovation in quantitative methods