Scientific Programmer Clinical - II (Associate)
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Scientific Programmer Clinical - II (Associate)
Ref No.: 18-08337
Location: North Wales, Pennsylvania
Title - Scientific Programmer Clinical - II (Associate)
Location - North Wales PA.
​Duration - 12+ Months 


Support the team by carrying out programming activities (as required), and to ensure timely, accurate programming and validation activities for clinical studies. Contributes to the overall efficiency, demonstrate the ability to work efficiently and to a high standard within a clinical team environment. Provides statistical programming and validation support for clinical study reports as well as coordinate programming activities among the study programmers to achieve timely progress in the following areas: CDISC ADaM datasets, statistical tables, figures, listings, electronic submissions and other internal and external requests (e.g., publications). Work independently to accomplish tasks and goals defined by programming lead.

Quals--
Qualifications: • Experience using SAS-Base, MACRO, STAT, GRAPH, MS Office. • Proven experience with transforming data in various formats (excel, csv, ascii) into SAS datasets. • Demonstrated ability to produce derived analysis datasets and TLFs using SAS 9.4 on a Window/UNIX environment. • Understanding of FDA guidelines and familiarity with the Clinical Trials process and CDISC data standards (SDTM, ADaM). Oncology experience preferred. • Good organization, time management and attention to detail. Must have skills needed to work in a stressful environment under tight deadlines while maintaining focus on details and quality. • Expected to conform to Client's SOPs and Programming practices. • Strong verbal, written and interpersonal communication skills needed to work effectively in a team environment. • Applies good judgment and demonstrates initiative to resolve issues. Experience & Education required: • BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field • Minimum 5 years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment. 3+ years' CDISC experience preferred. • Some project experience in a pharmaceutical/CRO programming environment or demonstrated significant leadership of SAS programming activities in a clinical pharmaceutical/CRO environment.