Clinical Research Nurse - Evening Shift

Quotient Sciences; Miami (FL); Vor Ort; USD 70.000 - 95.000; Vollzeit

Zusammenfassung

Quotient Sciences in Miami, FL seeks an experienced nurse to coordinate clinical research activities. You will administer study medications, monitor adverse events, and supervise unit staff while ensuring data quality and patient safety per GCP standards.

The role requires a Florida RN license, ACLS certification, and strong communication skills; bilingual English/Spanish is preferred. You will work closely with monitors and CROs and participate in study meetings and source documentation reviews.

Qualifikationen

• BSN or RN with critical care or clinical research experience.
• Current Florida nursing license.
• Current ACLS certification.
• Fluent in English/Spanish preferred.
• Proficient with Microsoft Office (Outlook, Word).

Aufgaben

• Administer study medication to participants and coordinate care.
• Monitor adverse events and ensure subject safety according to protocol.
• Supervise staff and study events on the unit; adjust staffing as needed.
• Maintain study schedules and review activities as they progress.
• Review and follow adverse events and ensure proper documentation.
• Confirm complete screening charts with informed consent and approvals.
• Interact with monitors and CROs regarding queries.
• Participate in key study meetings (SIV, kickoff, etc.).
• Ensure source documents are available and complete.
• Respond to medical emergencies and assist with other nursing duties.

Kenntnisse

Excellent communication

Attention to detail

Interpersonal skills

Bilingual English/Spanish

Ausbildung

BSN or RN

Tools

Microsoft Office

Jobbeschreibung

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
• Additional Tasks/responsibilities
• Assists with new employee (regular and per diem) training by providing orientation to general study procedures and responsibilities

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

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