Working as a Data Scientist with Real-world Clinical Data
Source category: Professional Development & Training
Author collections: Berber Snoeijer
THE COMMUNITY ARCHIVE
Clinical Programming Papers and PresentationsPage 49
Clinical programming connects study data, standards, analysis and reporting. Explore implementation papers on clinical trials, validation and repeatable workflows, then follow a focused topic for a particular dataset or deliverable.
981 papers · Showing 961–980
WPP, Worst Programming Practice - Real-life Pittfalls in Everyday Clinical Programming: Why and How
Source category: Industry Starters
Author collections: Hannes Engberg Raeder · Rowland Hale
A How-To Guide for Extending Controlled Terminology Using SAS Clinical Data Integration
Source category: Data Standards
The publisher lists this presentation but provides no paper file.
Author collections: Melissa Martinez
An Integrated platform to manage Clinical data, Metadata and Data Standards
Source category: Data Standards
The publisher lists this presentation but provides no paper file.
Author collections: Peter Wang
Careers in Biostatistics and Clinical SAS® Programming: An Overview for the Uninitiated
Source category: Career Planning
Author collections: Justina M. Flavin
Challenges in Processing Clinical Lab Data
Source category: Industry Basics
Author collections: Alan Meier
Clinical Data Dashboards for Centralized Monitoring Using SAS® and Microsoft® SharePoint®
Source category: Data Visualization and Graphics
Author collections: Jagan Mohan Achi
Clinical Study Report Review: Statistician’s Approach
Source category: Industry Basics
Clinical Trial Data Integration: The Strategy, Benefits, and Logistics of Integrating Across a Compound
Source category: Applications Development
Author collections: Keith Hibbetts
Clinical Trial Data Transparency: Seeing is Believing
Source category: Industry Basics
The publisher lists this presentation but provides no paper file.
Author collections: Janet Stuelpner
Common Variables in Adverse Event and Exposure analysis datasets specific for Oncology clinical trials
Source category: Industry Basics
Creating Define-XML version 2 with the SAS® Clinical Standards Toolkit 1.6
Source category: Data Standards
Author collections: Lex Jansen
Dealing with Missing Data in Clinical Trials
Source category: Applications Development
Author collections: Lucheng Shao
Handling with missing data in clinical trials for time-to-event variables
Source category: Statistics & Pharmacokinetics
Author collections: Giulia Tonini · Simona Scartoni · Angela Capriati
Methodology for Non-Randomized Clinical Trials: Propensity Score Analysis
Source category: Statistics & Pharmacokinetics
Monitoring Quality, Time and Costs of Clinical Trial Programming Projects using SAS®
Source category: Management and Support
Author collections: Jagan Mohan Achi
Risk-Based Approach to Identifying and Selecting Clinical Sites for Sponsor’s Preparation for FDA/EMA Inspection
Source category: Beyond the Basics
Author collections: Xiangchen (Bob) Cui
Risk-Based Monitoring of Clinical Trials Using JMP® Clinical
Source category: JMP
Author collections: Richard C. Zink
Techniques of Preparing Datasets for Visualizing Clinical Adverse Events
Source category: Data Visualization and Graphics
Author collections: Amos Shu · Qinghua (Kathy) Chen
The New Tradition: SAS® Clinical Data Integration
Source category: Applications Development
Author collections: Janet Stuelpner