RN Coord Clinical Research - Cardiology - Days na INTEGRIS Health
INTEGRIS Health · Oklahoma City, Estados Unidos Da América · Onsite
- Professional
- Escritório em Oklahoma City
INTEGRIS Health, Oklahoma’s largest not-for-profit health system has a great opportunity for a RN Coordinator Clinical Research in Oklahoma City, OK. In this position, you’ll work 8a-5p, Full-time, with our Cardiology team providing exceptional care to those who have entrusted INTEGRIS Health with their healthcare needs. If our mission of partnering with people to live healthier lives speaks to you, apply today, and learn more about our increased compensation plans and recently enhanced benefits package for all eligible caregivers such as front-loaded PTO, 100% INTEGRIS Health paid short-term disability, increased retirement match, and paid family leave. We invite you to join us as we strive to be The Most Trusted Partner for Health.
The RN Coordinator Clinical Research is responsible for the identification, consent process, consent randomization, administration of study drugs. Monitors eligible patients enrolled in research protocols in accordance with FDA required Good Clinical Practice.
Adheres to National Patient Safety Goals as appropriate based on the level of patient contact this position requires. INTEGRIS is an Equal Opportunity/Affirmative Action Employer. All applicants will receive consideration regardless of membership in any protected status as defined by applicable state or federal law, including protected veteran or disability status.
Responsibilities
The RN Coordinator Clinical Research responsibilities include, but are not limited to, the following:
- Responsible for specific clinical research studies as assigned by the Clinical Research Manager. It includes the identification, consent process, randomization, administration of study drugs, data collection/completion and monitoring of eligible patients enrolled in research protocols in accordance with FDA required Good Clinical Practices.
- Prepares documents for submission to the appropriate IRB and new protocol submissions, amendments, revisions, status changes, continuing reviews, expedited reviews and informational items. Maintains clinical trial regulatory files. * Identifies patients for clinical studies. Means include but are not limited to: chart reviews, physical assessments, advertising, health fairs, and phone
- Screening to determine study eligibility and enrolls appropriate patients in clinical studies to meet contractual goals
- Collects data as required by the study protocol including vital signs, ECGs, phlebotomy, and lab processing.
- Administers drugs according to protocol and inventories study drug to maintain drug accountability.
- Maintains research records including source documents, case report forms, and system EMR.
- Prepares for and participates in sponsor monitoring visits, study initiation visits, and closeout visits.
- Tracks and maintains the quality and integrity of all research trials.
- Reports to the Research Supervisor (ICIO)
- This position may have additional or varied physical demand and/or respiratory fit test requirements. Please consult the Physical Demands Project SharePoint site or contact Risk Management/Employee Health for additional information. Exposed to variations in volume and timing of work.
- May be required to work extended hours, on off shifts and weekends. Able to respond to a variety of demands and expectations from staff, physicians, patients and families. Exposure to high stress caused by a need to meet a variety of deadlines and priorities with constant interruptions from phone calls and co-workers.
- Exposure to automobile traffic and weather conditions when driving to and from doctor offices. Most travel is conducted between high volume times of day. Hazards are minimal if safety precautions are utilized.
- Work involves potential exposure to infectious waste, hazardous materials, exertion and musculoskeletal injury. May be exposed to cleaning solvents.
- All applicants will receive consideration regardless of membership in any protected status as defined by applicable state or federal law, including protected veteran or disability status.
Qualifications
- Current LPN license or licensure as a Registered Nurse (RN) in the State of Oklahoma or current multistate license from a Nurse Licensure Compact (eNLC) member state.
- Knowledge of medical terminology and intermediate computer and word processing skills.
- Must be able to communicate effectively in English (Verbal/Written).
- Research experience and Certified Clinical Research Coordinator preferred .
- Drivers License as well as a driving record which is acceptable to our insurance carrier.
- ICIO Wellness Center Only: Bachelors degree in related field may substitute for current professional license or Clinical Research Coordinator degree program.
