Registered Nurse

Description

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 the 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.