Principal Statistical Programmer sought by Parexel International LLC. Reporting to HQs in Newton, MA to conduct statistical analysis. Telecommuting permitted from anywhere within the U.S. up to 5 days/week.
Required: Master's degree in Pharmaceutical Science or a related field + 2 years of statistical programming experience. Must have at least 2 years of experience in each of the following: (1) statistical analysis & statistical support for clinical research questions on clinical trial data in an FDA 21 CFR part 11 regulated environment; (2) analyzing Statistical Analysis Plans (SAPs); (3) statistical analysis & statistical programming using SAS; (4) performing quality control on process & technical activities related to derived statistical datasets, table, listings, & figure programming in accordance with corporate quality standards, ICH-GCP, & regulatory requirements within Phase I-IV clinical trials; (5) evaluating & preparing project start-up activities, including project area set-up, creation of global programs, tracking spreadsheets, & required documentation; (6) utilizing SAS/BASE, SAS/STAT, SAS/SQL, SAS/MACRO, SAS Data Set, Proc Step, & Functions to generate statistical reports, tables, & listings; & (7) building structured CDISC, SDTM, & ADaM statistical datasets for clinical studies.
Annual salary: $142,911.20 - $207,400. To apply, send resume to [email protected] & cite requisition number 00934 or apply at jobs.parexel.com.
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