Clinical Research Nurse (Night)
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. Why join us: Because 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. 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
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 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
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
