Clinical Research Nurse - Per Diem Evening

Quotient Sciences•Miami, FL

8d•Onsite

About The Position

Quotient Sciences is a leading drug development and manufacturing accelerator, helping biotech and pharma companies bring new medicines to patients faster. With over 35 years of experience and a track record of success, we provide Drug Product (CDMO) and Clinical (CRO) services across the entire development pathway, including formulation development, clinical pharmacology, clinical trials, and commercial product manufacturing. Our proprietary and disruptive platform – “Translational Pharmaceutics®” – integrates Drug Product Manufacturing and Clinical Testing to eliminate silos in the drug development process. This in turn reduces costs, improves outcomes, and significantly accelerates drug development times. Every day counts when bringing new medicines to patients. Our 1,000+ experts across the US, UK, and beyond are united by science, agility, and a culture that turns ideas into impact—fast.

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.
Fluent in English/Spanish preferred.
Computer proficient in Microsoft Office products (e.g. Outlook, Word).
High attention to details.
Excellent communication and interpersonal skills.
Must be aged 18 years or over.
Must not have been debarred by the FDA.

Nice To Haves

Familiar with intravenous infusion techniques including pumps.
Familiarity with crash cart emergency procedures.

Responsibilities

Coordinating, supervising and monitoring study activities, following adverse events and administering study medications.
Complying and adhering to GCP guidelines and regulations as required of this role.
Ensuring study data is collected to a high quality in accordance with Good Clinical Practice (GCP) standards.
Ensuring subject safety at all times.
Administering study medication to study participants.
Supervising staff and study events on the unit according to protocol requirements.
Making staff adjustments during absences or other 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 interacting with pharmaceutical company representatives (monitors) and clinical research organizations (CRO) in response to queries during the course of the research study.
Participating in key study meetings- SIV, Clinical Kick-off, paperwork review, dummy run and as required.
Assuring that all necessary source documents are available on the unit on a timely basis.
Reviewing study source documents for completion.
Responding to medical emergencies in clinic and to adverse events requiring urgent attention.
Assisting with other nursing duties as assigned.
Assisting with new employee (regular and per diem) training by providing orientation to general study procedures and responsibilities.