Senior SAS Programmer Analyst

Integrated Resources, Inc

Woodcliff Lake, New Jersey

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JOB DETAILS

JOB TYPE

Contractor

SKILLS

Analysis Skills, Biostatistics, Biotech and Pharmaceutical, Clinical Data Interchange Standards Consortium (CDISC), Communication Skills, Computer Programming, Contract Research Organization (CRO), Data Sets, Detail Oriented, Employee Retention, FDA (Food and Drug Administration), Interpersonal Skills, Microsoft Windows Operating System, Multitasking, Organizational Skills, Phase III Clinical Trials, Presentation/Verbal Skills, Problem Solving Skills, Project/Program Management, Regulations, SAP, Software Development Lifecycle (SDLC), Statements on Auditing Standards (SAS), Statistical Analysis System (SAS), Statistics, Strategic Planning, Surveillance, Talent Management, Team Player, Technical Writing, Time Management, Unix Operating Systems, Writing Skills

LOCATION

Woodcliff Lake, New Jersey

POSTED

1 day ago

Senior SAS Programmer AnalystIntegrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.Job DescriptionThis position is responsible for supporting the phase 3 clinical trial, including but not limited to, as outlined below:Reviews SAP, TLG shells and variable derivation rules and provides feedback.Develops Study Quality Surveillance Plan and monitors study conduct to proactively address issues to ensure high quality study data.Develops the Data Monitoring Committee charter in collaboration with other functions and liaises with independent statisticians.Reviews the SAP, provides feedback to the statistician and develops (with the statistician) study specific dataset specs.Performs and validates statistical analysis.Independently reviews CSRs and performs data interpretation.Supports submission strategy planning, regulatory communication and development of Health Authorities responses.QualificationsMS in Biostatistics/Statistics preferred, with at least 5 years of experience in the pharmaceutical, CRO or biotech industry.Strong SAS programming skills, with experience in SAS-Base, MACRO, STAT, and GRAPH.Strong CDISC data standards, e.g. SDTM and ADaM.Good technical writing skills.Good communication skills with strong verbal, written and interpersonal communication skills.Strong organizational skills with ability to effectively manage multiple projects.Strong teamwork ability/commitment and individual initiative.Proven experience with UNIX and Windows operating systems.Understanding of the software development life cycle.Understanding of FDA guidelines.Good organization, time management and attention to detail skills.Needed to work in a stressful environment under tight deadlines while maintaining focus on details and quality.Applies good judgment and demonstrates initiative to resolve issues.

About the Company

Integrated Resources, Inc

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