Clinical Informatics Coordinator is responsible for the creation, implementation, and analysis of data and information systems required for patient care initiatives. Works with healthcare providers to identify useful clinical data and establish methods of collecting and storing it. Being a Clinical Informatics Coordinator performs analyses to create insights and identify patterns and areas for improvement. Communicates with providers and management to learn the organization's processes and priorities, and to provide takeaways in the most accessible and convenient way possible. Additionally, Clinical Informatics Coordinator typically requires a bachelor's degree. Typically reports to a manager or head of a unit/department. The Clinical Informatics Coordinator work is generally independent and collaborative in nature. Contributes to moderately complex aspects of a project. To be a Clinical Informatics Coordinator typically requires 4-7 years of related experience. (Copyright 2024 Salary.com)
Clinical Research Coordinator IIMedicine - Tulane Research Innovation for Arrhythmia Discoveries
Location: New Orleans, LA
SummaryThe Clinical Research Coordinator II will coordinate and conduct the day-to-day operations of TRIAD ongoing studies in cardiovascular diseases.
The Clinical Research Coordinator II is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by federal regulations.
As the primary resource for protocols, the Clinical Research Coordinator acts as a liaison between the patient, investigator, Institutional Review Board and sponsor.
The Clinical Research Coordinator II screens, enrolls and follows study patients, ensuring protocol compliance, and effective monitoring of clinical trial subjects.
The Clinical Research Coordinator II is also responsible for all data and source documentation, adverse event reporting and maintenance of complete regulatory files.
*Bachelor's Degree in public health or other science area or RN with current state licensure at the time of hire and one (1) year of related work experienceOR*LPN with current state licensure at the time of hire and four (4) years of related work experience; OR*Master's Degree in a related field
Preferred Qualifications*Knowledge of IRB submission process and requirements.
*Knowledge of good clinical practices as set forth by federal regulations.
About the Company:
Tulane University
Clear All
0 Clinical Informatics Coordinator jobs found in La Place, LA area