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HOSPITAL CORPORATION OF AMERICA Coordinator of Clinical Trials in Kansas City, Missouri

DESCRIPTION SHIFT: No WeekendsSCHEDULE: Full-time Do you have the career opportunities as a Coordinator of Clinical Trials you want in your current role? We have an exciting opportunity for you to join Research Medical Center a facility that is part of the nation's leading provider of healthcare services Company . At RMC we want to ensure your needs are met. We offer a variety of comprehensive medical, dental, and vision plans along with some unique benefits including: * Tuition Reimbursement/Assistance Programs * Paid Personal Leave * 401k 100% annual match - 3%-9% of pay based on years of service * Identity Theft Protection discounts * Auto, Home, and Life Insurance options * Adoption Assistance * Employee Stock Purchase Program ESPP We are seeking a Coordinator of Clinical Trials to ensure that we continue to provide all patients with high quality, efficient care. Did you get into our industry for these reasons? We are an amazing team that works hard to support each other and are seeking a phenomenal addition like you who feels patient care is as meaningful as we do. We want you to apply now! ABOUT THIS POSITION: The Coordinator of Clinical Trials is responsible for collaborative support andoversight of assigned clinical research trials to meet accrual targets, facilitate accurate data collection and quality performance. He/she is the primary point of contact for operational issues during active study conduct. RESPONSIBILITIES: * Partners with the treating physician to screen potential patients for protocol eligibility * Participates in the informed consent process, and completes execution of ICF * Coordinates patient care in compliance with protocol requirements * May deliver oral investigational product and drug diaries, performing pill counts as appropriate * Support patient teaching regarding administration of investigational product * Work with the physician to document any changes in patient condition, adverse events, concomitant medication use, protocol compliance, response to study drug * Responsible for accurate and timely data documentation and maintenance of patient records * Participates in monitoring visits and audits as requested * Participates in required training and education programs * Collaborates with Investigational Pharmacist to provide education for clinic staff regarding clinical research trials * Identifies quality and performance improvement opportunities and collaborates with leadership in the development of action plans to improve quality * Monitors patient laboratory data and communicates with physician regarding study requirements related to dose modification and adverse event reporting QUALIFICATIONS WHAT QUALIFICATIONS YOU WILL NEED: * Associates degree in a clinical or scientific related discipline required, Bachelor's degree preferred. * Relevant work experience may be substituted for educational requirements. * Registered Nurse preferred - Active Kansas/Missouri Nursing License * Clinical Research Certification CCRC, or CCRP, or eligible to obtain certification within the first year. * Minimum 3 three years of clinical research experience with exposure to oncology desirable. * Knowledge of medical terminology, nursing assessment, clinical trials and GCP * Experience with computer data entry and database management. * Excellent written and oral communication skills. * Excellent organizational skills, with high degree of attention to details and accuracy * Ability to read, analyze, and interpret technical procedures such as protocols, informed consent documents, and regulatory documents. * Demonstrates adaptability: Handles day to day work challenges confidently; is willing and able to adjust to multiple demands, shifting priorities, ambiguity and rapid change; shows resilience in the face of constraints, frustrations, or adversity; demonstrates flexibility. * Uses sound judgment to make timely, sound decisions; under conditions of uncertainty. * Shows work commitment: Sets high standards o