Screening Research Technician
Listed on 2026-08-29
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Healthcare
Clinical Research, Medical Technologist & Lab Technician
Posted Thursday, August 20, 2026 at 10:00 AM
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.
The Role- Currently hiring for a Temporary Technician to support Day shift
- To follow protocol guidelines for the preparation, collection, transfer, storage and shipping of all screening specimens according to protocol requirements and OSHA/State of Florida biohazardous regulations.
- To collect biological samples, performs phlebotomy, vital signs and ECG’s in accordance with the specific activity schedule.
- 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.
- Attends protocol training meetings to review specimen processing requirementsandensuresavailabilityofsuppliesneeded.
Coordinatesserviceswithany central lab involved in thestudy. - Performs study procedures including vital signs, ECGs, and sample collection in compliance with study protocols and SOPs.
- Notifies Screening Nurse of any vital sign, ECG or laboratory parameters that may exclude volunteer from study.
- Completes source documents following GCP and GDP standards. Must comply withall relevantSOPs.
- Performsqualitycontrolchecksforlabrequisitions.
- Reportseventsregardingthedamageorlossofasampleorincidences involving spillage or employee injury.
- Recordsthetemperatureofallfreezersandrefrigeratorsontheappropriate temperature logs on a daily basis.
- Verifiesthatallbiohazardousmaterialsaredisposedofappropriately.
Ensures proper labeling and preparation of biohazardous waste for transport. - Prepares specimens for shipping and adheresto regulations for biological sample shipping.
- Arranges overnight/express shipping of specimens and maintains related shipping documents.
- Receivesandsortsalllaboratorytestresultsforreviewbythe Investigatorsandclinical staff.
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