Lead SAS Clinical Programmer-Wilmington, DE - Georgia IT Inc.
Wilmington, DE
About the Job
Job Title : Lead SAS Clinical Programmer
Location : Wilmington, DE
Position Type : 12 Months Contract
Rate : DOE $50/hr on W2
Interview Process : Phone then Face to Face
U.S. Citizens, Green Card
Job Responsibilities:
Minimum Requirements:
Location : Wilmington, DE
Position Type : 12 Months Contract
Rate : DOE $50/hr on W2
Interview Process : Phone then Face to Face
U.S. Citizens, Green Card
Job Responsibilities:
- Conduct statistical programming work of clinical data using SAS Version 9 or above
- Ensure that all programs, outputs and documentation are consistent with ICH guidelines and are conducted in compliance with company SOPs.
- Participate in the review of 'Statistical Analysis Plan' and other documents essential to the conduct of statistical programming work for clinical trials;
- Generate analysis datasets according to CDISC standard and SAP
- Implement analysis methods according to SAP, and produce summary tables, graphs and data listings using SAS. Conduct adhoc analyses.
- Validate programs and associated results produced by other programming colleagues.
- Work with Clinical Research Organizations, as required, to participate in the oversight and management of programming activities to help ensure quality, timeline and deliverable are met;
- Develop standard SAS macros for efficient analyses of clinical data supervised by senior programmers
- Function as lead programmer in individual project teams for oversight of timeline, quality, and delivery.
- For Levels II and III, participate in TLF shell preparation and review, and assist statistician for SAP preparation
Minimum Requirements:
- BA/BS degree
- Minimum 5 years of programming experience using SAS Base/Stat/Macro/GRAPH in the biopharmaceutical and/or CRO industries; a MS in statistics or computer sciences is preferred for Levels II and III.
- Data Management experience and knowledge of CDISC standard are highly desirable
- Good SAS programming skills and attention to detail are essential
- Demonstrated knowledge of regulatory biostatistics, SOPs, and guidelines.
- Highly motivated and able to work well independently as well as being a good team player
- Strong organizational, time management, communication and project coordination skills for Levels II and III. The Level III position will typically be responsible for several studies concurrently, and supervise the day-to-day activities of programmers assigned to the project
- Must be able to hands-on and work well under timeline pressure.
Source : Georgia IT Inc.
