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Research Nurse Coordinator - Totowa, United States - Hackensack Meridian Health
Description
OverviewOur team members are the heart of what makes us better.
At Hackensack Meridian Health we help our patients live better, healthier lives — and we help one another to succeed.
With a culture rooted in connection and collaboration, our employees areteam members. Here, competitive benefits are just the beginning. It's also about how we support one another and how we show up for our community. Together, we keep getting better - advancing our mission to transform healthcare and serve as a leader ofpositive change.
The Research Nurse Coordinator is responsible for ensuring that the clinical research is conducted according to the research design including, but not limited to screening and recruitment of patients, collecting and records of clinical data, maintaining regulatory binders and overall safety of human subjects.
A day in the life of a Research Nurse Coordinator at Hackensack Meridian Health may include:
Assists in the preparation of new protocols
Assures that all protocol revisions, informed consents, continuing reviews, serious adverse events are reported in a timely manner
Acts as liaison between principal investigators and sub-investigators on all regulatory issues and changes within the protocol
Facilitates all audits of study with staff of Hackensack University Medical Center, sponsor, FDA, and other regulatory agencies
Reviews studies for feasibility and for competing protocols prior to submitting study
Reviews study with principal investigator to determine standard vs. research costs and assists in budget preparation
Screens subjects/patients for entry criteria, coordinates subject/patient schedules with investigators, and protocol schedules
Performs vital signs, and handles and ships lab specimens as outlined in the clinical program
Assists investigator with consent process assuring patients understand clinical trials
Monitors response to treatment and for any adverse events
Reports all serious adverse events to sponsor and IRB
Maintains accurate, complete, up-to-date records on each patient participating in a clinical protocol
Prepares for sponsor monitor site visits and ensures all supporting documentation records are adequate and available for the visit
Develops case report forms and/or databases for in-house studies as needed
Assists the principal investigator in data collection for writing abstracts, papers, and presentations
Provides education to all departments and clinical areas where study is performed
Adheres to the American Nurses Association standards
Identifies the needs of the patient population served and modifies and delivers care that is specific to those needs (i.e., age, culture, hearing and/or visually impaired, etc.).
Adheres to the standards identified in the Medical Center's Organizational Competencies.
Qualifications
Education, Knowledge, Skills and Abilities Required:
Graduate of a NLN/AACN accredited program in nursing
3-5 years clinical nursing experience
Mandatory education on human subjects research
Licenses and Certifications Required:
NJ State Professional Registered Nurse License
Licenses and Certifications Preferred:
Job ID
Department JTCC Hennessy Institute
Site Hackensack University Med Cntr
Job Location US-NJ-Totowa
Position Type Full Time with Benefits
Standard Hours Per Week 40
Shift Day
Shift Hours 8 a.m. - 4:30 p.m. /flex
Weekend Work No Weekends Required
On Call Work No On-Call Required
Holiday Work No Holidays Required
