statistical programmer

Responsibilities and Requirements: Experience working in various disease areas. They also must have specific expertise in SDTM programming, have submissions experience, and MUST possess strong skill in graphing. They need to be comfortable working as a strong independent contributor who is attentive and speaks up throughout the project work. Minimum of 5...

Job DescriptionCandidate to develop standard global data review tools, such as patient profiles, data quality checks, exception reports, PD reports, listings and figures for oncology trials.Ensure timelines and adequate quality of data review reporting deliverables for assigned trials. Follow processes and adhere to Client and project specific standards as...

Responsibilities: The SAS/Statistical Programmer will also be responsible for ensuring the accuracy and consistency of clinical data. The successful candidate will work closely with the Biostatisticians, Data Managers, and Clinical Research teams to develop and implement programming solutions to support clinical data analysis and reporting ...

Responsibilities: Ensure departmental or functional training plans in place and appropriate Perform vendor qualifications regarding statistical programming functions and manage CRO programming issues and activities to ensure on time deliverables within budget Generate, validate, and/or review SDTM domains and ADaM datasets and...

Build our future together:At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Principal Statistical Programmer to join our Statistical Programming team, supporting a study team across our clinical portfolio. In this role, you will provide programming leadership and support for...

Required Knowledge, Skills and Abilities: Experience as technical team lead directly engaging clients and coordinating tasks within a programming teamIn-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines?Knowledge of statistics,...

The Principal Statistical Programmer will lead programming activities for one or more studies, ensuring high-quality development, validation, and delivery of complex analysis outputs. Drive technical excellence, innovation, and standards adoption while providing strategic insights into study data. Mentor junior programmers and influence programming...

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. Create statistical analysis outputs to be used in support of final reports, abstracts,...

Company DescriptionArtech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution...

Responsibilities: Provides SAS programming support to all clinical studies. Manages assigned programming CROs providing oversight and appropriate QC for programming deliverables. Provide statistical programming support for regulatory submissions (e.g., FDA, EMA), including electronic submission standards (eCTD). Provides primary...

Job Description: We are seeking a highly motivated and qualified individual to join our Clinical Department as a Senior Statistical Programmer and work as part of a team to drive success. Ideal candidates will be self-motivated, independent, committed to the generation of high-quality data within a fast-paced and innovative research team. ...

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. Create statistical analysis outputs to be used in support of final reports, abstracts, posters,...

  Statistical Programmer -Contract Beaufort CRO seeks an experienced Statistical Programmer for contract based work. The Statistical Programmer’s duties include SAAS programming and analysis for one or more particular life science client projects, including clinical trial studies within the in-vitro diagnostic (IVD), medical device and...

Job DescriptionMinimum 2-3 years of experience defining SAS analysis requirements and performing SAS programmingBASE SAS certExpert knowledge of base SAS and SAS Macros for SAS software developmentDesign, development and unit-testing od SAS program code, functions and scripts to efficiently extract, merge and manipulate dataExpert Knowledge of lookup...

Job Summary: The Contract Lead Programmer serves as a senior, hands-on programmer responsible for managing statistical programming activities across multiple clinical trials and therapeutic areas. The role oversees external CRO partners to ensure high-quality, timely, and compliant delivery of analysis datasets, tables, listings, and figures that...

Responsibilities: Ensure departmental or functional training plans in place and appropriate Perform vendor qualifications regarding statistical programming functions and manage CRO programming issues and activities to ensure on time deliverables within budget Generate, validate, and/or review SDTM domains and ADaM datasets and associated...

Responsibilities: Ensure departmental or functional training plans in place and appropriate Perform vendor qualifications regarding statistical programming functions and manage CRO programming issues and activities to ensure on time deliverables within budget Generate, validate, and/or review SDTM domains and ADaM datasets and...

Company OverviewRhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases. We recognize the courage it takes for patients and their caregivers to begin their journey of advocacy to find the...

Responsibilities: Lead the development, validation, and documentation of CDISC-compliant SDTM and ADaM datasets for CNS clinical trials, ensuring traceability from raw data through analysis outputs. Program and QC tables, listings, and figures (TLFs) for interim and final clinical study reports, regulatory submissions, and client deliverables. ...

Responsibilities: Following the Study Data Tabulation Model (SDTM) Implementation Guide, writes specifications for SDTM datasets. Following statistical analysis plans and the Analysis Data Model (ADaM) Implementation Guide, writes specifications for analysis datasets. Following specifications, develops algorithms and writes programs to...