Research Nurse Coordinator

Location

Hackensack, NJ | United States

Job description

Our 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 are team 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 of positive 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 includes:

• 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.). This process includes communicating with the patient, parent, and/or primary caregiver(s) at their level (developmental/age, educational, literacy, etc.).
• Adheres to the standards identified in the Medical Center's Organizational Competencies.

Education, Knowledge, Skills and Abilities Required:

• Graduate of a NLN/AACN accredited program in nursing. 
• At least 3 years clinical nursing experience.
• Mandatory education on human subjects research.

Licenses and Certifications Required:

• NJ State Professional Registered Nurse License. 

If you feel that the above description speaks directly to your strengths and capabilities, then please apply today!

Job tags

Salary