's degree in life sciences, clinical data management, information technology, or a related field. An advanced degree...
Responsibilities and Requirements: Computer System Validation in addition to validation and regulation experience, the resource should have the following Experience: 3-7 years of relevant experience; can work independently and guide ment...
Responsibilities: Working under the direction of the Team Lead / Project Manager, the senior statistical programmer conducts programming activities for a trial, early phase project, indication, or publication activities Lead at least one...
Responsibilities: Prepare and submit CTAs within the EU Clinical Trial Integrated System (CTIS) and MHRA Integrated Regulatory Submission (IRAS) submission portals in accordance with regulatory requirements, using Submission Management to...
Responsibilities & Requirements: Responsible for preparing and executing test documentation for GMP computerized systems as well as providing support in the troubleshooting of issues during test execution. You should have an excellent u...
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. Cr...
Responsibilities: Generate and validate TLFs based on the Statistical Analysis Plan, TLF specifications, and industry best practices. With minimal oversight, perform all programming activities and documentation for assigned studies. F...
Responsibilities and Requirements: Experience in Tealium. JavaScript and React experience. Experience in Tagging on a website. Responsible for preparing and executing test documentation for GMP computerized systems as well as providing...
Responsibilities: Lead the creation of the Data Review and Cleaning Plan and development of the data cleaning strategy. Provide oversight of the data validation plan and provide DM insight to maximize the data validation strategy. Review...
Responsibilities and Requirements: Experience in Tealium. JavaScript and React experience. Experience in Tagging on a website. Responsible for preparing and executing test documentation for GMP computerized systems as well as providing...
Responsibilities: Lead the creation of the Data Review and Cleaning Plan and development of the data cleaning strategy. Provide oversight of the data validation plan and provide DM insight to maximize the data validation strategy. Revie...
Responsibilities : Responsible for preparing and executing test documentation for GMP computerized systems as well as providing support in the troubleshooting of issues during test execution. Should have excellent understanding of 21 CFR...
Responsibilities and Requirements: Responsible for preparing and executing test documentation for GMP computerized systems as well as providing support in the troubleshooting of issues during test execution. You should have excellent und...
Responsibilities: Remote for the right candidate. As a Contractor, Senior Clinical Data Manager, you will act as the point of contact for Data Management (DM) activities for multiple trials, provide oversight of data collection and manag...