وظائف مبرمج SAS سريري في الولايات المتحدة

Role: Sr. Data Engineer Skills Matrix attached- must be completed in DETAIL and returned with submittal Key Responsibilities Design develop and optimize robust ETL/ELT pipelines using Databricks Python and SQL. Write clean efficient and reusable code in SQL & Python for data tra المزيد...

Details:Stefanini Group is hiring!Stefanini is looking forSAS Programmers for 100% Remote work.For quick Apply please reach out to Ghanshyam Sharma- /Open for W2 Candidates only!Shift Schedule: Morning - US time zone 8 hours/dayThe Statistical Programming Contractor 3 is responsible f المزيد...

Responsibilities: Develop and maintain SAS programs to import clean and validate clinical trial data. Use R for data manipulation analysis and visualization. Perform statistical analyses in accordance with study protocols and analysis plans. Generate tables listings and figures (TLFs المزيد...

Responsibilities: Providing statistical programming support to generate tables listings and figures for assigned projects. Demonstrating proficiency in CDISC SDTM and ADaM to support various submission activities including IA CSR DSUR and publications. Overseeing all aspects of stati المزيد...

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 (TF المزيد...

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 (TF المزيد...

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. Contribut المزيد...

Responsibilities: Effectively manage and oversee statistical programming resources including contractors and CROs related to statistical programming deliverables to ensure high-quality within timeline and budget. Conduct hands-on validation/QC of CRO deliverables to ensure high-quali المزيد...

Responsibilities: The Principal SAS Programmer will be responsible for statistical programming for the clients clinical studies. In this role you will develop and validate SAS programs for data presentation analyses and provide programming support to project team members. Our Ideal c المزيد...

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 (TF المزيد...

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) المزيد...

Responsibilities: Providing statistical programming support to generate tables listings and figures for assigned projects. Demonstrating proficiency in CDISC SDTM and ADaM to support various submission activities including IA CSR DSUR and publications. Overseeing all aspects of stati المزيد...

Responsibilities: Position leads complex studies in study design statistical analysis and interpretation of results with some supervision. This position contributes to specific aspects of drug development plans with minimal supervision and contributes to documents submitted to Health المزيد...

Responsibilities: Providing statistical programming and validation support for clinical study reports overseeing programming activities by external vendors (e.g. CROs) when necessary and coordinating programming activities among the study programmers to achieve timely progress in the المزيد...

Responsibilities: Review protocols for CDISC conformance. Review Case Report Forms and eCRFs with CDISC CDASH and SDTM conformant elements. Write and manage SAS code for mapping clinical data to SDTM data structures in conformance with Emmes SDTM Implementation Guide project standard المزيد...

Responsibilities: The Sr. SAS Programmer will be responsible for statistical programming for the clients clinical studies. In this role you will develop and validate SAS programs for data presentation analyses and provide programming support to project team members. Our Ideal candida المزيد...

Responsibilities:The Sr. SAS Programmer will be responsible for statistical programming for the clients clinical studies.In this role you will develop and validate SAS programs for data presentation analyses and provide programming support to project team members.Our Ideal candidate w المزيد...

Responsibilities: Conduct statistical programming and analysis of clinical research studies. Provide programming support for publication efforts and regulatory submissions. Manage the timely creation review completion and delivery of statistical programming activities and deliverable المزيد...

Current Employees:If you are a current Staff Faculty or Temporary employee at the University of Miami please click here to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position using the Career worklet please review this tip s المزيد...

Responsibilities:Design code and test SAS programs used to generate CDISC SDTM & ADaM domains and tables listings & figures outputs.Perform analyses defined in the statistical analysis plan as well as ad hoc analyses as requested.Validate CDISC SDTM and ADaM data sets by using المزيد...