clinical sas Jobs

Refine Results
1 - 20 of 52 Jobs

Clinical SAS Programmer

Nityo Infotech Corporation

•

Raleigh, North Carolina, USA

Full-time

Job Role: Clinical SAS Programmer Job Location: Raleigh, NC/ Bridgewater, NJ/Hartford, CT Job Type: Full Time Job Description: Clinical SAS Programmer Required Skills & Experience: 5+ years of combined experience in SAS and R programming in the clinical research or pharmaceutical domain. Strong expertise in SAS programming for clinical data analysis, including SDTM, ADaM, and TLF programming. Proficiency in R programming for clinical data processing and visualization. Hands-on experience wit
Easy Apply
Posted 1 day ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

•

Boston, Massachusetts, USA

Full-time

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 and validates tables, figures, and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements. Provides input in the design and development of case report forms and clinical databases. Perf
Posted 29 days ago | Updated 7 hours ago

Sr. Clinical SAS programmer

Katalyst Healthcares and Lifesciences

•

Indianapolis, Indiana, USA

Full-time

Responsibilities: Perform data manipulation, analysis, and reporting of clinical trial data. Develop and maintain department/system-level macros. Create and review SDTM and Adam specifications. Create and validate SDTM data sets. Create and validate analysis data sets. Create and validate patient profiles. Program and generate tables, figures, and listings (TFLs). Validate and document SAS programs and outputs. Fulfil ad-hoc analysis requests. Provide other services. Requirements: Bachelor's deg
Posted 21 days ago | Updated 7 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

North Chicago, Illinois, USA

Full-time

Responsibilities: Liaise with stakeholders to understand clinical study data aggregation requirements. Use the analytics platform to set up the study for the processing of data from source and/or systems. Load data from EDC, and extract into the analytics platform map to SDTM and/or other custom data formats. Understand the protocol and eCRF document and prepare the SDTM specification. Interact with the study team to understand the study requirements. Understand and identify data loading options
Posted 5 days ago | Updated 7 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

Bridgewater, New Jersey, USA

Full-time

Responsibilities: Lead and participate in the development and validation of high quality CDISC datasets based on the implementation guides and consultations with sponsors, project leads, systems analysts, other programmers, and end users. Use your expertise in data standards and regulatory requirements to lead discussions with clients about appropriate approaches to database design. Use study protocol, CRF, Data Transfer Agreements from vendors, data sources, CDISC CT, TAUGS, and CDISC implement
Posted 32 days ago | Updated 7 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

Irving, Texas, USA

Full-time

Responsibilities: Performing data manipulation, analysis, and reporting of clinical trial data for both safety and efficacy (ISS/Client) utilizing SAS programming. Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures ( TLFs). Production and QC / validation programming. Ability to program from scratch and able to handle complicated domains and TLF's. Ability to read and apply protocol and SAP. Demonstrate good understanding of the endpoints and d
Posted 34 days ago | Updated 7 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

South San Francisco, California, USA

Full-time

Responsibilities: Performs all SAS programming required for clinical trial analysis and reporting. Ensures that activities and processes performed are conducted according to sponsor requirements. Works closely with the Biostatistics and Data Management departments on various clinical projects. Designs and/or reviews database structure. Writes edit checks from the Data Cleaning Plan (DCP) specifications. Creates derived-analysis datasets. Executes analyses specified in the Statistical Anal
Posted 34 days ago | Updated 7 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

Chicago, Illinois, USA

Full-time

Responsibilities: Lead the design, development, and maintenance of the MHN Analytic Platform. Manage, mentor, and ensure technical and analytical development of a team of analysts. Work with teams to operationalize analytic and reporting innovations. Evaluate BI and machine learning solutions. Identify opportunities for process improvement. Requirements: 6 + years of experience using Base SAS, SAS/Macros, and SQL required. Subject matter expert in healthcare data, with 5 + years
Posted 34 days ago | Updated 7 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

San Diego, California, USA

Full-time

Responsibilities: Manage programming activities on project or study level, including managing CROs to ensure deliverables are accurate and compliant. Act as a Programming SME for assigned studies, including authoring/reviewing programming specifications, such as SDTM/ADaM specifications, TFLs creation and QC for reporting events, ESUB packages, and documenting production and validation programs. Apply programming skills to support statistical analysis, clinical reporting, regulatory submission
Posted 34 days ago | Updated 7 hours ago

SAS Clinical Trails Programmer

Katalyst Healthcares and Lifesciences

•

Cary, North Carolina, USA

Full-time

Responsibilities: The consultant will provide programming/analytical support utilizing client as the primary programming language to create and manage the production of analysis reports. summary tables/listings and graphs for clinical trials submitted to various regulatory bodies worldwide. The consultant must have excellent communication skills and must be able to communicate about the techniques developed and results of analysis both to executives and other analysts in the organization. Pe
Posted 34 days ago | Updated 7 hours ago

Business Analyst | Hybrid | Chicago | Contract to Hire

Walker Healthforce

•

Remote

Contract

Business Analyst| Hybrid | Chicago, IL|Contract to Hire Walker Healthforce is seeking a Business Analyst with to support a healthcare clientbased out of Chicago, IL. This is a 6-month contract to hire opportunity. RATE RANGE: $41 - $43 START DATE:June 16, 2025 HOURS/SCHEDULE: M-F; 8AM - 5PM CST WORKER TYPE: Full-Time CORE REQUIREMENTS: Strong experience in writing complex SQL queries to extract and validate data from the database. Proficient in creating and executing SQL queries in Oracle, SA
Easy Apply
Posted 8 days ago | Updated 8 days ago

SAS Programmer

Katalyst Healthcares and Lifesciences

•

San Diego, California, USA

Full-time

Responsibilities: Serves as lead programmer for assigned projects to provide statistical and programming support in one or more Phase I- clinical studies. Design and perform quality checks on analysis datasets, tables, listings, figures (TFL), and written reports to support clinical trial results using SAS. Create and review annotated CRF to STDM datasets. Produce and maintain technical programming specification documents. Lead and actively participate in client and project review meetings.
Posted 25 days ago | Updated 7 hours ago

Senior Data Analyst

Zachary Piper Solutions, LLC

•

Remote

Full-time

Piper Companies is seeking a Senior Data Analyst to join a global leader in clinical research and healthcare analysis for a remote position . The Senior Data Analyst w ill lead statistical programming and analysis for oncology observational studies, managing complex datasets, ensuring quality control, and collaborating with scientists to drive meaningful insights from real-world evidence. Responsibilities of the Senior Data Analyst include: Lead statistical programming and analysis using oncolo
Posted 4 days ago | Updated 17 hours ago

Senior Manager Data Management

Katalyst Healthcares and Lifesciences

•

San Diego, California, USA

Full-time

Responsibilities: Responsible for data management documentation, including, but not limited to data management plan(DMP), CRF, eCRF design, edit check specifications, data issue logs, and data review plans and ensures all documents follow study design and regulatory requirements. Maintain Data Management outsourcing metrics and key performance indicators to aid the selection of CRO partners / Vendors and the ongoing management of partnerships. Participate in vendor qualifications and audits.
Posted 34 days ago | Updated 7 hours ago

Data Scientist I - Wagner Lab

University of Pittsburgh

•

Pittsburgh, Pennsylvania, USA

Full-time

The Data Scientist's primary responsibilities will include curating data, assessing data integrity, facilitating the use of effective data management tools, and analyzing clinical research data following traumatic brain injury and other acquired neurological injuries. The incumbent should have proficient knowledge in at least one statistical software package (e.g. SAS) and some working knowledge of other packages (e.g. SPSS, R). The incumbent should have some working knowledge of SQL database st
Posted 60+ days ago | Updated 7 hours ago

Senior Clinical Data Analyst

Katalyst Healthcares and Lifesciences

•

Boston, Massachusetts, USA

Full-time

Job Description: This position focuses on assisting with analysing data and deriving insights from clinical and safety data sources to generate evidence and support decision making across the organization. The Associate will leverage a variety of analytics and visualization techniques to contribute to research, clinical development, drug safety and post-marketing activities. Responsibilities: Collaborates and works closely with cross-functional teams, including data analysts/engineers and busin
Posted 14 days ago | Updated 7 hours ago

Senior Consultant - Clinical Data Programming

Veeva Systems

•

Raleigh, North Carolina, USA

Full-time

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead. At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company - we made history in 2021 by becoming a public benefit corporation
Posted 38 days ago | Updated 8 hours ago

Clinical Data Analyst

Katalyst Healthcares and Lifesciences

•

Irvine, California, USA

Full-time

Responsibilities: The main function of a clinical data analyst is to create moderately complex metrics to identify trends in data and remediation, utilizing tools (e.g., systems, reports) to assess the need for training and provide basic recommendations to improve data status during study conduct. Evaluate data errors and collection issues; provide guidance and recommendations to the clinical team for resolution. Define and specify clinically data collection requirements (e.g., eCRFs, CRFs, ed
Posted 34 days ago | Updated 7 hours ago

Data Analytics Leader

Software Guidance & Assistance

•

South San Francisco, California, USA

Contract

Software Guidance & Assistance, Inc., (SGA), is searching for a Data Analytics Leader for a direct placement assignment with one of our premier Pharmaceutical Services clients in South San Francisco, CA. Responsibilities : The Data Analytics Leader (DAL) in gRED Early Clinical Development (ECD) Data Intelligence team supports ECD study teams by delivering timely and high-quality analysis and real-time interactive visualizations. The DAL is an expert in data analysis and data insights, enabling
Posted 56 days ago | Updated 5 hours ago

Prin Clin Data Scientist (Data Mgr)

Novartis

•

Hanover

Full-time

Job Description Summary Location: East Hanover, NJ Onsite (cannot be done remotely) Hiring for multiple roles. About the role: Love clinical data management? Bring that passion to Novartis! This key Principal Clinical Data Scientist will be responsible and accountable for managing all Data Management deliverables at a consistently high standard with respect to cost, quality, and timelines for all assigned indications within one or more Global Clinical Program(s)/Project(s). Job Description
Posted 58 days ago | Updated 7 hours ago