Deputy Lead

Quotient Sciences:
Molecule to Cure. Fast.

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.

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.

• 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

• Supports the Clinical Leads by providing leadership, encouragement, support and positive reinforcement within the clinical team
• Deputizes for the Clinical Lead during periods of absence in all aspects of the role including line management
• Understands resource (staffing) requirements for assigned studies
• 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 administering study medication to study participants
• Familiar with intravenous infusion techniques including pumps
• Responsible for timely reviewing, recording and following adverse events
• Responds to medical emergencies in clinic and to adverse events requiring urgent attention
• 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
• Paticipates 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 and performs quality control checks on study source documents for completion, accuracy, and compliance to GCP and protocol
• Facilitates clinical training and reassessment of core clinical competencies (e.g. venipuncture, cannulation, safety assessments, holter monitoring, etc.)
• Supports training for both new and existing members of clinical team; assists with new full time and per diem employee training by providing orientation to general study procedures and responsibilities
• Ensures all members of clinical team are fully trained and signed off in relevant SOP/competency before working unsupervised or on a study
• Familiarity with crash cart emergency procedures
• Troubleshooting and problem solving as directed by Clinical Lead
• Assists with other nursing duties as assigned

• BSN or RN with at least 6 months experience of working in a clinical research environment or equivalent experience in another role
• 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, Excel, PowerPoint)
• High attention to detail
• Excellent communication and interpersonal skills

• 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

When applying for a position with Quotient Sciences to be able to work in our organization you must be aged 18 years or over and not have been debarred by the FDA. If you indicate you are under the age of 18 or have been debarred then your application will be automatically declined.

Quotient Sciences are advocates for positive change and conscious inclusion. We strive to create a diverse Quotient workforce and develop a workplace culture that provides a sense of…