Paramedic Per Diem (Evening / Night)

Quotient Sciences

Miami (FL)

On-site

USD 60,000 - 90,000

Full time

14 days+
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Job summary

Quotient Sciences in Miami, FL seeks a qualified clinical professional to supervise volunteer safety, collect samples, and manage study procedures. The role requires phlebotomy experience, ACLS/BLS certifications, and adherence to OSHA and GCP standards.

Strong communication and attention to detail are essential for success during inpatient stays. The position involves monitoring vital signs, performing ECGs as trained, and ensuring proper data recording and adherence to study protocols while

Qualifications

  • Paramedic license and relevant certifications required.
  • ACLS and BLS certification required.
  • Minimum two years of active phlebotomy experience preferred.
  • Knowledge of OSHA regulations and proper blood collection techniques.
  • Excellent attention to detail and strong communication skills.

Responsibilities

  • Monitor volunteer safety through telemetry within scope of practice.
  • Respond to medical emergencies and follow directives within scope of practice.
  • Collect biological samples (blood, urine, stool, etc.) per study schedule.
  • Record and maintain blood draws and other specimen data per SOPs.
  • Draw blood by venipuncture according to study schedules and labels.
  • Ensure unit is prepared with necessary supplies and equipment.
  • Maintain a clean, safe clinical environment and adhere to SOPs.

Skills

Attention to detail
Communication
Interpersonal skills
Clinical directives compliance

Education

Paramedic license
ACLS certification
BLS certification
Phlebotomy experience
OSHA knowledge

Job description

The Role
  • Responsible for the supervisionand monitoring of volunteer safety through telemetrymonitoringwithin scope of practice
  • To collect biological samples, performs phlebotomy, vital signs andECG’sin accordance withthe specific activity schedule
  • To track overall study event schedule and participant compliance
  • Tocomply and adhere to GCP guidelines and regulations as required of this role
  • To ensure study data is collected to a high qualityin accordance withGood Clinical Practice (GCP) standards
  • Toensuresubject safety at all times
Main Tasks and Responsibilities
  • Responsible for the monitoringof 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 forcollection of biological samples; e.g. blood, urine, stool, sputum
  • Responsible fordrawing blood specimens (by venipuncture) according to the times specified in the study schedules
  • Responsible for recording andmaintainingrecords of blood draws and other biologicalspecimen collections (per SOPs) via paper or electronic forms
  • Assistwith the proper labelling and preparation of blood collection tubes when indicated
  • Assures that all necessary blood collection tubes,equipmentand supplies are on thefloor 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 andrecordsvital signsaccurately; recognizesandreports any abnormal vital signs accordingly
  • OperatesECG machine, performs ECGs, and/or works withholtermonitors 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 forassistingin the recording and distributing of meals to study participants according to strict meal schedules
  • Assures that the unit iskept clean and orderly at all timesand removes any items notpermittedfrom the floor
  • Able to interact andmaintaina professional demeanour with study participants during their inpatient stay
  • Responsible forobservingconfidentiality practicesregardingany protocols, subjectinformationand/or any relevant industry informationat all times
  • Assistswith the preparation of data collection binders and study documents as assignedby the Clinical Research Nurse
  • Assistswith any other duties as assigned
Job Demands

The job may involve the following:

  • Very highconcentration 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
  • Current/Valid Paramedic license
  • Current Advanced Cardiac Life Support (ACLS) and Basic Life Support (BLS) certification
  • Minimum two years of active phlebotomy experience preferred
  • Required to have working knowledge of OSHA regulations and proper bloodcollection techniques (evaluable during employee orientation period)
  • Able to follow medical directives
  • High attention to details
  • Excellent communication and interpersonal skills

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