<Back to Search
Clinical Trial Management System (CTMS) Specialist - OnCore
Saint Paul, MNMarch 25th, 2026
Clinical Trial Management System (CTMS) Specialist – OnCoreLocation: Remote, must be in the U.S.Openings: 10+, including Lead Specialists openingsDuration: Contract (Through June 1)Start Date: ASAPPosition OverviewWe are seeking an experienced CTMS Specialist with strong proficiency in OnCore to support a critical data migration project tied to our newly implemented CTMS. This role will focus on transferring clinical trial calendar and budget information from Excel into OnCore, ensuring accuracy, compliance, and readiness for go-live optimization.Key ResponsibilitiesTransfer study calendar data from Excel into OnCoreMigrate and validate budget data within OnCore financial modulesPerform quality control (QC) to ensure data accuracy and integrityIdentify and resolve discrepancies between legacy Excel files and OnCore configurationCollaborate with clinical operations, finance, and IT stakeholdersSupport go-live readiness activities, including validation and testingEnsure alignment with institutional SOPs and regulatory compliance standardsDevelop documentation and provide knowledge transfer as neededRequired QualificationsDemonstrated hands-on experience with OnCore CTMSExperience building and managing study calendars within OnCoreStrong knowledge of clinical trial budgeting workflows and build in OnCoreAdvanced proficiency in Microsoft ExcelStrong understanding of clinical research operationsExcellent attention to detail and data validation skillsAbility to work independently in a fully remote environment
Showing 450 of 35,636 matching similar jobs
- Senior Specialist, Scientific Affairs
- Clinical Research Coordinator
- Clinical Research Associate- Oncology
- SAP FI/CO Analyst - S/4HANA Migration & Enhancements
- Associate Director, Clinical Quality Assurance
- Regulatory Affairs Lead, Electric Utilities (Hybrid TX)
- GCP Quality Governance Lead: Operations & Risk
- Senior Director, Regulatory Affairs CMC
- Senior IT Compliance & Governance Leader (GxP)
- Principal Regulatory Affairs Specialist - Cardiac Ablation
- Senior Systems Analyst (Lead)
- Hybrid Clinical Research Protocol Coordinator
- Clinical Research Site Manager 248787
- Clinical Research Site Manager 250509
- Associate Director, Clinical Quality Compliance
- Director, Business Management & Strategy for HNW Clients
- Clinical Research Site Director - 248142
- Clinical Research Coordinator
- Senior Clinical Research Coordinator - Accellacare (Cary, NC)
- Remote Trial Data Domain Lead
- Mergers and Acquisitions Specialist
- Sr Manager, Product Strategy (Digital Health)
- Senior Manager, US Advertising and Promotion Lead Pharmaceutical
- Senior Medical Science Liaison, Neurodegeneration (NDG) Pipeline (Northeast)
- Clinical Research Coordinator
- Director, Quality and Regulatory Affairs
- Project Manager - Medical Affairs
- Quality & Compliance Director: GMP & Regulatory Lead
- Regulatory Specialist
- Senior Clinical Research Coordinator
- Medical Affairs Manager, Compliance - III*
- Clinical Research Coordinator
- Clinical Research Coordinator
- Clinical Research Coordinator
- Quality & Health Innovation Project Lead (Hybrid)
- Quality Systems Manager, Clinical Lab GxP
- Clinical Data Manager
- Global Regulatory Strategy Director
- Medical Science Liaison - EST/CST
- Senior Medical Science Liaison - Hematology (California and Hawaii)