DescriptionJOB SUMMARYThe Registered Nurse, or LPN, 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.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.
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