Offer summary
Qualifications:
MSc/PhD in pharmacoepidemiology/biostatistics or equivalent experience, Substantial experience in related environments, Proficiency with R or SAS required, Knowledge of CDISC and OMOP is a plus, Fluent in English, written and spoken.
Key responsabilities:
- Provide expertise in statistical methods and theories
- Design and report RWE and clinical research studies
- Ensure compliance with regulatory guidelines and quality processes
- Mentor study team on statistical methodologies
- Oversee and approve all statistical deliverables of assigned studies