Clinical Data Manager, CSRN

Clinical Data Manager, CSRNVirginia Commonwealth UniversityBenefits: All full-time university staff are eligible for VCU's robust benefits package that includes comprehensive health benefits, paid annual and holiday leave granted up front, generous tuition benefits, retirement planning and savings options, tax-deferred annuity and cash match programs, employee discounts, well-being resources, abundant opportunities for career development and advancement, and more.Continuing education for undergraduate and graduate tuition for a maximum of 6 credits per semester; Professional development opportunities encouraged and offered for employees as part of annual career development, e.g. certifications, seminars, courses, annual conferences, mentorship; 28 Vacation Days, 12+ State Holidays, and 4 Days to volunteer; Medical, Dental and Vision Health Benefits to meet the needs of employees and their eligible family members from the Commonwealth of Virginia as well as optional FSA; Participation in the Virginia Retirement System (VRS) and other retirement saving options; Parental and Caregiver Leave, Short Term Disability (STD), Disability Insurance, Voluntary Long Term Care Insurance, and Employee Assistance Program.Unit: Massey Comprehensive Cancer Ctr MBUDepartment: Massey Clinical Trials OfficeDepartment Summary: Massey Comprehensive Cancer Center Mission: To reduce the state cancer burden for all Virginians by addressing the confluence between biological, social, and policy drivers through high-impact, cutting-edge research; person-centered care across the continuum, from prevention through survivorship; community integration; and training the next generation of community-centric researchers and healthcare professionals Vision: To be a premier community-focused cancer center leading the nation in cancer health equity research and ensuring optimal health outcomes for allPosition Primary Purpose and General ResponsibilitiesClinical Data Managers generally perform administrative and study related duties that are essential to the successful management of research conducted by principal investigator(s) at the university. This position may support human subject research that is not conducted in a clinical or health care environment or does not require access to clinical facilities, systems, or data. Typical duties may include scheduling and monitoring of research activities and timelines; coordinating the management, storage, and reporting of study data; monitoring data to maintain quality control; and scheduling and booking monitoring visits. They may work independently or as a member of a team. They work under general supervision, resolving most standard issues independently and referring complex issues to an upper-level manager. Clinical Data Managers typically report to a manager or director or may report to a department administrator. NOTE: Maintain established portfolio driven knowledge base of federal and state laws and regulations, sponsor guidance as well as university policies and compliance notices, with ability to consistently interpret and apply accurately.This recruitment is open for three (3) separate Clinical Data Manager positions.Job Description:Assist with participant recruitment, enrollment, tracking, data collection, and verification of data in the study databaseMaintain understanding of clinical research management duties from study initiation to closeoutMaintain current CITI credentials for Human Subjects Protections, Good Clinical Practice (GCP), and additional certifications as requiredEngage in various forms of communication about the studies they are assistingUnderstand and adhere to all IRB requirements, Human Subjects Protection regulations, and all aspects of the IRB approved protocolCoordinate and ensure access for monitoring and auditing visitsResponsible for all data entry of protocol required visits and proceduresRespond to data queries as assignedAssigned to assist different teams based on resource needsClean up any prior data discrepanciesAssist with sample preparation, collection and processing as neededCollect survival follow-up data on applicable participantsComply with VCU Health's (VCUH) clinical research clinical permissions tableEnsure compliance and adherence to clinical research protocolsEnsure studies are audit readyEnsure all study data is captured in OnCore and comply with department policiesFollow VCU internal processes to ensure compliance with VCU policies related to research activities and ensure compliance with federal and state regulatory standardsOther duties as assignedQualifications:Minimum QualificationsHigh School Diploma or equivalentMust be able to complete mandatory competencies and certifications required by VCU and VCU H, individual clinical trials and the NIH Human Subjects Protection trainingCandidates whose resumes highlight the following previous experience will be prioritized:Demonstrated experience working in and fostering an environment of respect, professionalism and civility with a population of faculty, staff, and students from various backgrounds and experiences, or a commitment to do so as a staff member at VCU;Advanced proficiency with data entry and word processing skills, with the ability to analyze and interpret information effectively;Advanced organizational abilities and a keen eye for detail to ensure accuracy and efficiency in all tasks with the ability to multitask and prioritize autonomously;Clear and professional written and verbal communication skills, with the ability to interact effectively with colleagues and stakeholders;Interpersonal skills, capable of building relationships and collaborating with team members at all levels to gather information and support compliance efforts;Problem-solving and organizational aptitude, with the ability to manage multiple tasks, meet deadlines in a dynamic environment and independently make critical decisions.Preferred QualificationsBachelor's degree or equivalent combination of training and experience preferredCertification from the Society of Clinical Research Associates (SOCRA), the Association of Clinical Research Professionals (ACRP) or CRA certification for Research Administration.Previous experience in oncology clinical research preferredSpanish speaking preferredPosition will remain open until filled. Applications received by November 6, 2026 will be given priority consideration.Salary Range: Commensurate with experience, range minimum of $44000FLSA Exemption Status: Non-ExemptRestricted Position: NoORP Eligible: NoFlexible Work Arrangement: HybridUniversity Job Title: 93406 - OpenContact Email: View email address on click.appcast.io agency within the Commonwealth of Virginia is dedicated to recruiting, supporting, and maintaining a competent and diverse work force. Equal Opportunity Employer