CDISC Jobs in California

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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 14 days ago | Updated 9 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 23 days ago | Updated 9 hours ago

Senior Manager Data Management

Katalyst Healthcares and Lifesciences

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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 23 days ago | Updated 9 hours ago

Assoicate Director of Clinical Data Science

Pivotal Solutions Inc

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Menlo Park, California, USA

Full-time

Qualifications Required: Master s or PhD in Data Science, Biostatistics, Computer Science, Life Sciences, or a related field10+ years of experience in clinical data programming or clinical data science within a pharmaceutical, biotech, or CRO environmentProficiency in R, SAS, or Python, and experience with data visualization tools (e.g., Shiny, Spotfire, Tableau)Strong understanding of clinical data standards (e.g., CDISC, SDTM) and clinical trial processesDemonstrated ability to collaborate wi
Easy Apply
Posted 28 days ago

Statistical Programmer Consultant

Tandym Tech

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Novato, California, USA

Contract

Our client, a leading Life Sciences Company, needs to hire a Statistical Programmer to provide programming support for Phase 1 to Phase 3 studies, including project integration and disease monitoring project work. This is a 6-month contract, 100% REMOTE. **Qualified candidates must be able to work on a W2 basis. Responsibilities: Provides timely support to the project team on all statistical programming matters according to the project strategy. Programs SDTM/ADaM/TLFs for the studies, write
Easy Apply
Posted 2 days ago | Updated 1 hour ago

Clinical Data Manager

Tandym Tech

•

Remote

Contract

A recognized pharmaceutical company has a great Remote opportunity awaiting a new Clinical Data Manager. In this role, the Clinical Data Manager will be responsible for contributing Data Management Support for assigned programs. The contractor is a self-motivated, collaborative clinical data management professional who is a self-starter and thrives in a fast-paced environment. Responsibilities: Work with the Clinical Data Management (CDM) Lead to support operational activities for one or more pr