Location: New York,NY, USA
DescriptionJOB SUMMARYThe Registered Nurse participates in the conduct of clinical trials, monitoring the 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 managemultiple 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 assignedExact compensation may vary based on skills, experience, and location. For NYC, the salary range is up to $50/ hr.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 of 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