Quotient Sciences · 2 weeks ago
Clinical Research Technician (with Phlebotomy experience) - Per Diem
Quotient Sciences is a leading drug development and manufacturing accelerator, helping biotech and pharma companies bring new medicines to patients faster. The Clinical Research Technician will be responsible for collecting biological samples, performing phlebotomy, and ensuring study data is collected in accordance with Good Clinical Practice standards while maintaining subject safety.
Clinical TrialsCommercialConsultingHealth CareManufacturingMedicalPharmaceutical
Responsibilities
Collects biological samples, performs phlebotomy, vital signs and ECG’s in accordance with the specific activity schedule
Tracks overall study event schedule and participant compliance
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
Responsible for collection of biological samples; e.g. urine, and sputum
Responsible for drawing blood specimens (by venepuncture) 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
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
Able to take and record accurate vital signs; recognize and report any abnormal vital signs
Able to operate ECG machine and or holter if within scope of practice
Promptly reports any study participant’s adverse event and/or lack of compliance to the Study Nurse Coordinator
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 Study Nurse Coordinator
Assists with any other duties as assigned
Qualification
Required
Technical school phlebotomy training or Medical Assistant certificate
Required to have working knowledge of OSHA regulations and proper blood collection techniques (evaluable during employee orientation period)
Collects biological samples, performs phlebotomy, vital signs and ECG's in accordance with the specific activity schedule
Tracks overall study event schedule and participant compliance
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
Responsible for collection of biological samples; e.g. urine, and sputum
Responsible for drawing blood specimens (by venepuncture) 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
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
Able to take and record accurate vital signs; recognize and report any abnormal vital signs
Able to operate ECG machine and or holter if within scope of practice
Promptly reports any study participant's adverse event and/or lack of compliance to the Study Nurse Coordinator
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 Study Nurse Coordinator
Assists with any other duties as assigned
Preferred
Minimum two years of active phlebotomy experience preferred
Company
Quotient Sciences
Quotient Sciences provides formulation development, clinical pharmacology, clinical & commercial manufacturing services.
Funding
Current Stage
Late StageTotal Funding
$35MKey Investors
TA Associates
2019-07-18Acquired
2008-09-03Private Equity· $35M
Recent News
FierceBiotech
2025-12-20
Company data provided by crunchbase