Senior Clinical Analyst and Programmer-Argentina
Core
Lead SAS programming activities to create data listings, safety reviews, and reports for clinical trial data review and centralized monitoring.
Role type
Senior Clinical SAS Programmer
Builds
SAS data review listings, safety review listings, and centralized monitoring reports
Domain
Clinical research / Biotechnology / Dermatology
Required skills
SAS programming, clinical trial data analysis, regulatory compliance knowledge, data validation, report generation, SOP development, mentorship
Preferred skills
Master's degree in CS/IT/Statistics/Engineering, SAS certification, advanced programming experience
Technologies
SAS
Responsibilities
Create listing specifications based on user requirements; Generate SAS Data Review Listings; Create Safety Review Listings; Support Centralized Monitoring reports; Document code and specification changes; Assist in developing data standard SOPs; Mentor junior analysts and programmers
Seniority
Senior, hands-on IC with mentorship responsibilities (via careerplan.io/jobs/15-003-27-37F-senior-clinical-analyst-and-programmer-argentina)