- Experience supervising and training research staff, including organizing, prioritizing, and scheduling work assignments in a clinical or medical setting.
- Excellent organizational, interpersonal, and communication skills, both verbal and written.
- Proficient in various software programs (including database management [e.g. Access], presentation packages [e.g. PowerPoint], spreadsheets [e.g. Excel], and advanced word processing [e.g. Word]).
- Ability to perform, manage, and balance multiple projects and tasks simultaneously, work under time constraints, and meet deadlines.
- Highly detailed and organized.
- Excellent work ethic.
- Ability to work independently and efficiently.
- Ability to maintain confidentiality in all work performed.
- Skilled in coordinating and organizing meetings and/or special events and willingness to assume additional duties when necessary.
- Highly organized and detail oriented in order to ensure all study procedures are completed as described in the study protocol, ensure participants are contacted at the correct date and time for the conduct of study assessments.
- Willing to travel occasionally to conduct patient home visits and to attend steering committee meetings.
- Bachelor's degree in epidemiology, public health, or other science area or RN with current Louisiana licensure at the time of hire.
- Three years' clinical research experience in conducting epidemiology research and clinical trials, including recruitment, coordinating research activities, and experience measuring blood pressure and anthropometrics.
- Master's degree in epidemiology, clinical research, or public health preferred.
- Certified Clinical Research Coordinator
- Clinical research experience in cardiovascular disease, hypertension, and renal disease.
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Senior Clinical Research Coordinator, Epidemiology - New Orleans, United States - Tulane University
Description
The Senior Clinical Research Coordinator will coordinate and oversee the day-to-day operations of epidemiology studies and clinical trials in cardiovascular and chronic kidney diseases.
The Senior Clinical Research Coordinator is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by federal regulations.
Specific responsibilities include managing research staff and conducting chart reviews, measuring blood pressure and anthropometric measurements, conducting non-invasive cardiovascular disease test procedures (e.g., electrocardiograms), and managing patient visits.
The Senior Clinical Research Coordinator is also responsible for all data and source documentation, adverse event reporting and maintenance of complete regulatory files.
