Principal Statistical Programmer
Scorpion Therapeutics
Role: Principal Statistical Programmer leading clinical trial data analysis and submission activities. Objectives include ensuring quality, compliance, and timely delivery of statistical outputs for clinical development programs. Responsibilities: Responsibilities cover SAS programming, quality control, supporting regulatory submissions (eCTD, ISS/ISE), and collaborating with cross-functional teams like Biostatistics, Data Management, and Regulatory Affairs. Requirements: Bachelor's in a Scientific discipline; 8+ years in biotech/pharma/clinical research with expertise in SAS, CDISC standards, and regulatory submissions. Preferred: advanced knowledge of clinical trial processes and regulatory standards. HighValue: extensive SAS proficiency, regulatory submission experience, validation of electronic data submissions, and compliance with FDA/ICH/GCP. Work setup: remote, hybrid, or onsite option with flexibility; no travel specified. #J-18808-Ljbffr
Vacancy posted 1 day ago
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