Clinical SAS Programmer

Responsibilities

• Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s)
• Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets
• Creates and validates tables, figures and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements
• Provides input in the design and development of case report forms and clinical databases
• Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs
• Programs quality checks for clinical study raw data and reports the findings to Data Management
• Reviews or author eCRF, SDTM and ADaM dataset specifications for programming
• Provides programming support for ad‑hoc analysis
• Identifies problems and develops global tools that increase the efficiency and capacity of the Statistical Programming group (e.g., macros or graphical user interface applications)
• Manages timelines and schedules of specific phases of projects with internal personnel and external vendors
• Acts as lead programmer for a study
• Reviews or validates statistical deliverables of vendors for assigned project(s)

• MS in Statistics, Computer Science, or a related field with at least 3 years or BS in Statistics, Computer Science, or a related field with at least 5 years
• Experience in providing statistical programming support to early and late phase clinical trials
• Excellent skills in SAS programming and statistical reporting
• Knowledge of CDISC standards for SDTM and ADaM and FDA electronic data submission requirements
• Familiarity with FDA and ICH regulations and guidelines
• Excellent problem‑solving skills
• Good written and verbal communication skills and organizational and documentation skills
• Ability to work on a multidisciplinary team that may include Biostatistics, Medical Directors, Data Management, Medical Writing, Pharmacovigilance, Clinical Operations, Medical Affairs, etc.
• Ability to prioritize and multi‑task effectively
• Demonstrated positive attitude and the ability to work well with others

Mid-Senior level

Contract

Information Technology

Pharmaceutical Manufacturing