Clinical Sas Programmer jobs

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...

DUTIES: Proficient to write SAS codes to produce CDISC complaint datasets. Create statistical analysis outputs to be used in support of final reports, abstracts, posters, manuscripts, adhocs and other clinical publications. Write QC SAS programs for Dataset, Tables...

Responsibilities: To support the Biostatistics team by carrying out programming activities of statistical programmers and overseeing external vendors (as required), and to ensure timely and accurate programming and validation activities for clinical studies and publications...

Our client, a leading Medical Device Manufacturing Company is looking for Statistics & Statistics Programming - Specialist - 3 / SAS Programmer and This is for an initial duration of 06 Months Contract Remote Role...

Responsibilities: To support the Biostatistics team by carrying out programming activities of statistical programmers and overseeing external vendors (as required), and to ensure timely and accurate programming and validation activities for clinical studies and...

Title: Elluminate Programmer / Clinical Data Programmer Location Remote Duration: 6 months + Extensions Responsibilities will include: Provides application administration and technical support as the subject matter expert on core business packages related...

Job Title:Clinical Programming Contractor Location:100% Remote Type:Contract Duration:Up to 2 year assignment Shift Schedule:Regular 40-hour work week (morning shift) Position Summary...

Title: Senior Statistical Programmer Duration: Jun 8 Dec 31, 2026 Location: Irvine, CA, 92618 Schedule: 1st Shift, 9:00 AM - 5:00 PM TECHNICAL SKILLS Must Have...

Responsibilities: Convert specifications into SAS code to generate datasets and Tables, Listings, and Figures outputs. Be responsible for overall project delivery, including clinical trial reports and other regulatory submission deliverables....

Bill? On site?Role Purpose Provide hands on statistical programming support for clinical studies, including development and validation of analysis datasets and statistical outputs, in accordance with regulatory and company standards. The Senior Statistical Programmer...

Title: Data Engineer (SAS Programmer) Location: Remote (EST / CST preferred) Duration: 6 Month Contract Our client is seeking a Data Engineer (SAS Programmer) to support SAS modernization efforts by analyzing existing workflows...

Position Purpose: The Senior Programmer for Data Validation supports cross-functional teams such as Statistics, Data Management and Standards by overseeing and ensuring the quality of clinical data build and programming activities across in-house, hybrid, and vendor-supported studies...

Responsibilities: The Senior Clinical Applications Systems Analyst Epic independently defines system objectives, requirements, scope, and impact based on needs of clinical operations. Develops or modifies clinical information technology procedures to solve complex healthcare problems, considers......

Responsibilities: The Senior Clinical Applications Systems Analyst Epic - Beaker independently defines system objectives, requirements, scope, and impact based on needs of clinical operations. Develops or modifies clinical information technology procedures to solve complex healthcare problems,......

The SAS to Python/R Migration Developer is responsible for hands-on conversion, testing, and validationof SAS analytical code into Python and/or R under the guidance of a migration architect. This role focuses on execution quality, code accuracy, and reproducibility. This is a build-and-deliver...

Our client, is a Banking company, is looking for a Oracle PL/SQL Developer with SAS for their Mainframe: Jersey City, NJ location. Responsibilities: Convert mainframe SAS process to Oracle SQL/PLSQL. Build Java UI for process maintenance. Build support...

Principal Programmer - Clinical Data Oversight & Standards provides leadership and oversight for clinical data build, programming, and vendor deliverables across in-house, hybrid, and outsourced studies, ensuring alignment with CSL standards, regulatory requirements, and industry best practices....

Sr. Principal Statistics needs 4 years (Ph. D) or 6 years (MS) Pharmaceutical/CRO industry experience Sr. Principal Statistics requires: SAS, ICH guidelines, CDISC data structures, FDA guidelines, SAP preparation, TFL shells, CRF review, database design review, edit check specifications...