Senior Global Regulatory Affairs Specialist
... clinical trials, interpreting complex medical data, and contributing to the advancement ...
... clinical trials, interpreting complex medical data, and contributing to the advancement ...
... to review and evaluate clinical data records. • Excellent communication and interpersonal ...
... maintaining complete, accurate and timely data and essential documents in systems ...
... clinical trials, interpreting complex medical data, and contributing to the advancement ...
... , Futility & Predictive Inference, Estimands, Missing Data etc.) Where required, ability to ...
... and for timely delivery of data to required quality. Leads Local ...
... CTA activities and analyze consolidated data Support budget development and workload ...
... program objectives, experimental design, and data analysis to meet regulatory and ...
... , ensuring that accurate and reliable data is generated to facilitate the ...
... clinical trials, interpreting complex medical data, and contributing to the advancement ...