7 regulatory coordinator jobs at 6 companies in Eldon, MO
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Clinical Research Coordinator I
Columbia, Missouri, United States
OnsiteFull Time
ObjectiveHealth: Integrates clinical research into physician practices via proprietary technology.
Full-time clinical research coordinator with patient care skills and experience managing IRB-approved trials; data entry, regulatory compliance, and study setup.
Human Subject Research Program/Project Support Coordinator II
Columbia, Missouri, United States
$23-$26/hrOnsiteFull Time
University of Missouri: Public university providing higher education, research, and healthcare services.
2+ YOEBachelor's degree or equivalent plus 2 years' related experience; coordinate human subject research operations, support budgets/feasibility, ensure data submission in REDCap/REDCap Cloud/OnCore, supervise research technicians, and maintain regulatory compliance.
Arrow Senior Living: Operating senior living communities with assisted and memory care.
3+ YOECurrent LPN or RN license in state of employment, 3+ years assisted living/resident care experience, medication and regulatory knowledge, ability to supervise staff, TB clearance, DOJ/FBI criminal clearance, good health and clean driving record.
StoneBridge Senior Living: Provides skilled nursing, assisted living, and memory care services.
3+ MgmtRegistered nurse with supervisory experience to lead nursing department, ensure regulatory compliance, manage budgets, coordinate care, and oversee staff development.
Fulton Manor Care Center: Providing 24-hour skilled nursing and rehabilitation services in Fulton.
2+ YOEMissouri RN license with leadership in skilled nursing, knowledge of care planning and MDS, strong documentation and regulatory compliance skills, staffing coordination, and analytical decision-making.
University of Missouri: Public university providing higher education, research, and healthcare services.
2+ YOEAssociate's degree (or equivalent) and 2+ years relevant experience; administrative skills including scheduling, calendar management, meeting coordination, data entry, regulatory documentation, and support for clinical research and program operations.