> Markdown version of [/jobs/ext/4332905-hybrid-research-systems-analyst-wvu-cancer-institute-clinical-research-unit](https://www.wearedevelopers.com/jobs/ext/4332905-hybrid-research-systems-analyst-wvu-cancer-institute-clinical-research-unit). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # (Hybrid) Research Systems Analyst - WVU Cancer Institute Clinical Research Unit - **Company:** West Virginia University - **Location:** Morgantown, WV, United States - **Experience:** Experienced - **Contract:** Permanent contract - **Skills:** Data Analysis, Software Applications, Software Documentation, Information Systems, Databases, System Configuration, Systems Theories, Network Troubleshooting, Microsoft Office, Microsoft SharePoint, Information Technology, User Accounts - **Published:** October 15, 2026 - **Apply:** https://jobs.localjobnetwork.com/apply/add/88646333/1 ## About the Role * Bachelor's degree in Health Sciences, Information Systems, Computer Science, Business, or a related field. * A minimum of two (2) years of experience in the following: + Clinical research, healthcare operations, information systems support, or a related area. * Any equivalent combination of related education and/or experience will be considered. * All qualifications must be met by the time of employment. Knowledge, Skills, and Abilities * Basic knowledge of clinical research and healthcare operations. * Ability to learn and support clinical research software applications. * Familiarity with GCP, HIPAA, FDA, and IRB requirements, or the ability to learn through training. * Proficiency with Microsoft Office applications. * Strong organizational, communication, customer service, and problem-solving skills. * Ability to manage multiple priorities and work effectively with technical and non-technical users. * Attention to detail and ability to maintain accurate records and documentation. Requirements * Completion of the OnCore Certification Program within one (1) year of hire, if required. * SoCRA Certified Clinical Research Professional (CCRP) certification preferred. ## Description The Cancer Institute Clinical Research Unit at West Virginia University is currently accepting applications for a (Hybrid) Research Systems Analyst. About the Opportunity The Research Systems Analyst provides support for clinical research systems used by the WVU Cancer Institute Clinical Research Unit (WVUCI CRU) and affiliated sites. Assists with the administration, maintenance, and day-to-day operation of clinical research applications, including OnCore, eReg, Analytics, EDC, and future systems. Serves as a resource for research staff by providing user support, maintaining system data and documentation, assisting with training, and supporting clinical research operations and compliance activities., * Assist with the administration and maintenance of clinical research systems. * Support testing, validation, and implementation of system upgrades and enhancements. * Manage user accounts, security access, and system-related documentation in accordance with established procedures. * Provide first-level support and troubleshooting for research staff and system users. * Develop and maintain training materials, job aids, and user documentation. * Perform data entry, data maintenance, and routine data quality reviews. * Assist research staff with study calendars, forms, templates, and system configuration activities. * Generate routine reports and assist users with reporting needs. * Communicate system issues and enhancement requests to vendors, IT teams, and leadership as appropriate. * Maintain sponsor, staff, institutional, and study records within research applications. * Assist with maintenance of SharePoint sites, shared drives, and other electronic resources. * Support technology onboarding activities for new employees. * Provide basic support for Microsoft Office applications and common hardware or network issues. * Participate in meetings, training activities, and quality improvement initiatives. * Maintain knowledge of clinical research systems, policies, and applicable regulatory requirements.