Clinical Research Nurse - Per diem Weekend

Quotient Sciences•Miami, FL

About The Position

The Role Responsible for coordinating, supervising and monitoring study activities, following adverse events and administering study medications To comply & adhere to GCP guidelines and regulations as required of this role To ensure study data is collected to a high quality in accordance with Good Clinical Practice (GCP) standards To ensure subject safety at all times Main Tasks and Responsibilities Responsible for administering study medication to study participants Familiar with intravenous infusion techniques including pumps Responsible for supervising staff and study events on the unit according to protocol requirements. Responsible for making staff adjustments during absences or others unanticipated work circumstances Responsible for monitoring study schedules and reviewing study activities as they progress Responsible for reviewing, recording and following adverse events Responsible for confirming that a complete screening chart containing informed consents, lab results and Investigator approval is available on the day of admission for every admitted subject Responsible for monitoring clinical results, compliance, and/or safety issues which would trigger the exclusion or discontinuation of a participant Ability to effectively interact with pharmaceutical company representatives (monitors) and clinical research organizations (CRO) in response to queries during the course of the research study Participates in key study meetings- SIV, Clinical Kick-off, paperwork review, dummy run and as required Assures that all necessary source documents are available on the unit on a timely basis Reviews study source documents for completion Familiarity with crash cart emergency procedures. Responds to medical emergencies in clinic and to adverse events requiring urgent attention Assists with other nursing duties as assigned Assists with new employee (regular and per diem) training by providing orientation to general study procedures and responsibilities The Candidate BSN or RN with experience preferably within a critical care setting and/ or clinical research environment Current/valid Florida nursing license Current Advanced Cardiac Life Support (ACLS) certification Fluent in English/Spanish preferred Computer proficient in Microsoft Office products (e.g. Outlook, Word) High attention to details Excellent communication and interpersonal skills Job Demands The job may involve the following: Very high concentration of work Strict and tight deadlines Having to juggle a range of tasks/issues simultaneously Working in a hazardous environment with high requirement to follow safety procedures Working outside normal working hours Needing to respond to client demands

Requirements

BSN or RN with experience preferably within a critical care setting and/ or clinical research environment
Current/valid Florida nursing license
Current Advanced Cardiac Life Support (ACLS) certification
Computer proficient in Microsoft Office products (e.g. Outlook, Word)
High attention to details
Excellent communication and interpersonal skills

Nice To Haves

Fluent in English/Spanish preferred

Responsibilities

Responsible for coordinating, supervising and monitoring study activities
Following adverse events and administering study medications
Administering study medication to study participants
Supervising staff and study events on the unit according to protocol requirements
Making staff adjustments during absences or others unanticipated work circumstances
Monitoring study schedules and reviewing study activities as they progress
Reviewing, recording and following adverse events
Confirming that a complete screening chart containing informed consents, lab results and Investigator approval is available on the day of admission for every admitted subject
Monitoring clinical results, compliance, and/or safety issues which would trigger the exclusion or discontinuation of a participant
Effectively interact with pharmaceutical company representatives (monitors) and clinical research organizations (CRO) in response to queries during the course of the research study
Participates in key study meetings- SIV, Clinical Kick-off, paperwork review, dummy run and as required
Assures that all necessary source documents are available on the unit on a timely basis
Reviews study source documents for completion
Responds to medical emergencies in clinic and to adverse events requiring urgent attention
Assists with other nursing duties as assigned
Assists with new employee (regular and per diem) training by providing orientation to general study procedures and responsibilities