Night Shift)

Quotient Sciences•Miami, FL

24d

About The Position

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. 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 the supervision and monitoring of volunteer safety through telemetry monitoring within scope of practice To collect biological samples, performs phlebotomy, vital signs and ECG’s in accordance with the specific activity schedule To track overall study event schedule and participant compliance To comply and 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

Current/Valid EMT-Paramedic.
Current Advanced Cardiac Life Support (ACLS) certification
Required to have working knowledge of OSHA regulations and proper blood collection techniques (evaluable during employee orientation period)
Able to follow medical directives
High attention to details
Excellent communication and interpersonal skills

Nice To Haves

Minimum two years of active phlebotomy experience preferred

Responsibilities

Responsible for the monitoring of volunteer safety as applicable through scope of practice
Able to respond to medical emergency and follow medical directives within scope of practice
Responsible for communicating any noted adverse within scope of practice
Adherence to applicable SOPs and Protocol
Responsible for collection of biological samples; e.g. blood, urine, stool, sputum
Responsible for drawing blood specimens (by venipuncture) according to the times specified in the study schedules
Responsible for recording and maintaining records of blood draws and other biological specimen collections (per SOPs) via paper or electronic forms
Assist with the proper labelling and preparation of blood collection tubes when indicated
Assures that all necessary blood collection tubes, equipment and supplies are on the floor prior to blood draw time
Prepares the unit for any scheduled activities and upon completion removes all equipment and/or supplies from the floor
Measures and records vital signs accurately; recognizes and reports any abnormal vital signs accordingly
Operates ECG machine, performs ECGs, and/or works with holter monitors if trained and within scope of practice
Promptly reports any study participant’s adverse event and/or lack of compliance to the Clinical Research Nurse
Must be familiar with proper phlebotomy and laboratory procedures in compliance with OSHA regulations, Good Clinical Practices and Quotient Sciences Operating Procedures
Responsible for proper biomedical waste disposal procedures and schedules
Responsible for reading and understanding all protocols and schedules
Responsible for assisting in the recording and distributing of meals to study participants according to strict meal schedules
Assures that the unit is kept clean and orderly at all times and removes any items not permitted from the floor
Able to interact and maintain a professional demeanour with study participants during their inpatient stay
Responsible for observing confidentiality practices regarding any protocols, subject information and/or any relevant industry information at all times
Assists with the preparation of data collection binders and study documents as assigned by the Clinical Research Nurse
Assists with any other duties as assigned