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Clinical Research Point Coordinator – Open Rank Intermediate to Senior
2 weeks ago
Clinical Research Point Coordinator – Open Rank Intermediate to Senior-37346University StaffDescriptionUniversity of Colorado Anschutz Medical CampusDepartment: Clinical Research Support Team (CReST)Job Title: Clinical Research Point Coordinator – Open Rank Intermediate to SeniorPosition #: 00827546 – Requisition #: 37346Job Summary:The Clinical Research Support Team (CReST) has an opening for a full-time Point to Senior Clinical Research Coordinator to provide regulatory, study coordination, and data collection/entry support for a variety of drug, device and biologic studies conducted at the University of Colorado Anschutz Medical Campus and affiliate hospitals. This position may act as lead or co-lead coordinator overseeing coordinating activities for assigned studies, and/or as a primary contact for training and guidance for junior coordinators supporting these studies. This position will have independent decision making and project management responsibilities. Knowledge of Good Clinical Practice and Good Documentation Practices in the context of clinical research is essential.We are seeking an individual who is collaborative, communicative, caring, detail oriented and organized, proactive, able to think critically, focused on quality, passionate about research, dedicated to personal growth, and highly motivated in all areas of study coordination.Key Responsibilities:Point level –Shepherds and completes study startup activities from initial site selection through budget negotiation, operationalization, organizational and regulatory approvals, and site activation to prepare completely for enrollment of the first study subject.Proactively seeks guidance and engages stakeholders to problem solve and push forward startup activities efficiently to meet sponsor timelines.Delegates startup tasks to other assigned team members and/or leadership to efficiently execute and meet timelines and milestones.Independently crafts and submits nursing orders for approvalModifies, or supervises modifications of Informed Consent Forms to comply with Institutional guidelines and obtains required approvalsCompletes and manages regulatory submissions to local and central IRBs, PRMS, and other regulatory bodies. Drafts regulatory documents and completes forms/paperwork. Fields questions and provides study-specific updates related to regulatory submissions and progressTrains and mentors junior staff, and serves as a reference point within CReST for questions and guidance related to their duties and assigned studies.Develops protocol-specific systems and documents including process flows, training manuals, source documents, Standard Operating Procedures (SOPs) and Case Report Forms (CRFs).Demonstrates and applies comprehensive working knowledge of applicable regulations, policies and GCP, and advises coworkers and study teams on compliance and application.Assists senior staff with more advanced tasksProvides feedback to CReST managers and leadership on billing and invoicing systems and related metrics.Senior level only –All entry and mid-level dutiesAdvises investigators on regulatory matters, best practices, and institutional policies. May develop or assist with development of research plans.Engages with essential research resource teams on campus, including UCHealth Research Admin, OnCore, pharmacies, labs, and clinics for study planning. Develops working relationships with key contacts to strategize on study startup and implementation.Independently project-manages full-service study startup. Negotiates Study Startup Agreements.May present on behalf of CReST or studies at University or external eventsOversees study closeout and archiving activitiesServes as a strategic partner and advisor to CReST leadership on development and implementation of SOPs and other standard work.Consult as needed with CReST leadership on the activities, status, metrics, and capabilities of the CReST coordinator program.Undertakes special projects in collaboration withThis description is a summary only and is describing the general level of work being performed, it is not intended to be all-inclusive. The duties of this position may change from time to time and/or based on business need. We reserve the right to add or delete duties and responsibilities at the discretion of the supervisor and/or hiring authority.Work Location:Hybrid – this role is eligible for a hybrid schedule of 4 days per week on campus and as needed for in-person meetings.Why Join Us
