Research Nurse Coordinator I (Hybrid)
About The Position
The Research Nurse Coordinator I is responsible for all activities associated with clinical study coordination, subject recruitment/enrollment, data management/integrity, regulatory compliance, project/study evaluation and interfaces with participants and family members. Coordinates the clinical logistics of the study, and works in tandem with the Research and/or Clinical Nurse who provide hands-on clinical care to research participants. Utilizes clinical nursing background and basic research protocol knowledge to serve as a liaison between nursing staff, Principal Investigator, other research staff, and study participants.
Requirements
- Associate. Degree/College Diploma Nursing required.
- 2 years of Clinical Nursing Experience required.
- RN State License California RN license Upon Hire.
- Basic Life Support Upon Hire.
Nice To Haves
- Bachelor's Degree Nursing or Health Science preferred.
- 1 year Clinical research experience preferred.
Responsibilities
- Responsible for clinical study activities, coordination, adherence to protocols and serves as a liaison between study participants, Principal Investigator (PI), and other research staff.
- Provides educational services to research participants and family regarding study participation, participants current clinical condition, and or disease process.
- Assesses and documents adverse events reported by research participants, informs PI, and documents according to department process (grade, attribution, treatment, etc), and reports to regulatory and sponsor as required.
- Records research data where assessed or reported by patient (i.e. symptoms of treatment).
- Presents education materials to the interdisciplinary team on study requirements.
- Collaborates with the interdisciplinary team and communicate a plan of care that allows for safe and effective collection of clinical research data.
- Schedules research participant study visits.
- Triages patient by phone and provides clinical information to the patient.
- Completes and documents study participant enrollment, assessment/reassessment, education, and follow-up activities.
- Coordinates study participant tests and/or procedures as required and ensures protocol is followed.
- May prepare IRB submissions.
- May process, ship, track or otherwise handle research specimens.
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What This Job Offers
Job Type
Full-time
Education Level
Associate degree
