Registered Nurse

Clinilabs; Eatontown (NJ); On-site; USD 62,000 - 69,000; Full time

Job summary

Clinilabs is seeking a Registered Nurse to contribute to clinical trials, monitor participant safety, and assist the study team with protocol execution. Responsibilities include protocol task execution, specimen collection, vital signs, ECGs, adverse event monitoring, and guiding junior staff.

The role requires an RN with NY/NJ license, ACLS training, and at least three years of clinical experience with telemetry in CCU/ICU settings; clinical trial experience is a plus.

Qualifications

• Must be a registered nurse with current NY/NJ license.
• BSN preferred.
• ACLS training required.
• Three years of clinical experience with telemetry in CCU/ICU; clinical trial experience preferred.

Responsibilities

• Time management to handle multiple projects and meet objectives.
• Read and execute protocol tasks.
• Perform blood sampling via angio-catheters and direct venipulture.
• Collect samples (urine, feces, timed urine) and obtain vitals.
• Perform ECGs and monitor adverse events.
• Provide clinical care during study participation and train/mentor new personnel.

Skills

Telemetry monitoring

Microsoft Office

Clinical research experience

Communication skills

Education

Bachelor of Science in Nursing

RN license (NY/NJ)

ACLS certification

Tools

Microsoft Office

Job description

Description

The Registered Nurse participates in the conduct of clinical trials, monitoring safety and well-being of the subjects, and assists the study team with all functions related to the execution of protocols.

Job Summary

The Registered Nurse participates in the conduct of clinical trials, monitoring safety and well-being of the subjects, and assists the study team with all functions related to the execution of protocols.

Responsibilities

• Time management techniques must be used to manage multiple projects efficiently to ensure specified project objectives, timelines, and quality requirements are met.
• Read and execute assigned protocol tasks.
• Insert angio-catheters for blood sampling and intravenous medication.
• Oversee and perform data collection in a manner that is consistent with Standard Operating Procedures, the study protocol, and the standards of GCP.
• Obtain required blood samples through angio-catheters and direct venipuncture.
• Perform sample collection of urine, feces, and timed urine collection.
• Obtain vital signs (blood pressure, heart rate, and temperature).
• Obtain medical history, height, and weight of subjects.
• Perform electrocardiograms.
• Monitor and manage adverse events through documentation of clinical observations.
• Monitor concomitant medications.
• Provide clinical care to subjects during study participation.
• Monitor activities of Medical Assistants, LPNs, and Study Assistants.
• Perform accurate and timely completion of case report forms (CRFs).
• Perform emergency and resuscitative interventions as appropriate.
• Assist in the training and mentoring of new personnel.
• Provide leadership in the CRU (in) absence of the Study Coordinator.
• Other duties as assigned

The salary for this position is $45-50/hr. Final compensation is based on skills, experience, location, and overall expertise.

Requirements

• Must have graduated from an accredited nursing program and be a Registered Nurse with a current NY/NJ license. A Bachelor of Science in Nursing is preferred.
• Training in Advanced Cardiac Life Support (ACLS) will be required.
• Three (3) years experience working in a clinical setting is required with extensive experience with telemetry monitoring in a CCU/ICU setting, and clinical trial experience is preferred.
• Must be familiar with Microsoft Office® products and possess computer skills necessary to deliver project objectives.
• Must be able to prioritize activities in a manner consistent with Clinical Research Unit goals: act with professionalism under adverse conditions, handle confidential information with discretion; work under minimum supervision to accomplish complex tasks; accept challenges and new responsibilities; actively manage the changing priorities and work distribution based upon needs of the unit; and assist the team to stay focused on objectives with results orientation.
• Must exhibit a positive work attitude and high productivity, consistently deliver on commitments, facilitate the work of the project team, and demonstrate excellent interpersonal skills.