ORS Partners
Phlebotomist
ORS Partners, Miami, Florida, us, 33222
Overview:
Company OverviewOur growing and successful business comprises of over 850 talented individuals globally, in an environment where everybody counts and is instrumental to our success. With state-of-the-art manufacturing and clinical facilities in the UK and USA, we deliver a full range of drug development solutions around the globe saving our clients both time and money.People join Quotient Sciences because we are a respected member of the drug development world, specializing in delivering innovative solutions that integrate formulation development, real time GMP manufacturing and clinical testing We pride ourselves on the quality of our services and our engaged culture. We are passionate about helping our customers get new medicines to market.The RoleCollects biological samples, performs phlebotomy, vital signs and ECGs in accordance with the specific activity scheduleTracks overall study event schedule and participant complianceTo ensure study data is collected to a high quality in accordance with Good Clinical Practice (GCP) standardsTo ensure subject safety at all times
Main Tasks and Responsibilities:Responsible for collection of biological samples; e.g. urine, and sputumResponsible for drawing blood specimens (by venipuncture) according to the times specified in the study schedulesResponsible for recording and maintaining records of blood draws and other biological specimen collections (per SOPs) via paper or electronicAssist with the proper labelling and preparation of blood collection tubes when indicatedAssures that all necessary blood collection tubes, equipment and supplies are on the floor prior to blood draw timePrepares the unit for any scheduled activities and upon completion removes all equipment and/or supplies from the floorAble 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 practicePromptly reports any study participants adverse event and/or lack of compliance to the Study Nurse CoordinatorMust be familiar with proper phlebotomy and laboratory procedures in compliance with OSHA regulations, Good Clinical Practices and Quotient Sciences Operating ProceduresResponsible for proper biomedical waste disposal procedures and schedulesResponsible for reading and understanding all protocols and schedulesResponsible for assisting in the recording and distributing of meals to study participants according to strict meal schedulesAssures that the unit is kept clean and orderly at all times and removes any items not permitted from the floorAble to interact and maintain a professional demeanor with study participants during their inpatient stayResponsible for observing confidentiality practices regarding any protocols, subject information and/or any relevant industry information at all timesAssists with the preparation of data collection binders and study documents as assigned by the Study Nurse Coordinator.Assists with any other duties as assignedAdditional Tasks / ResponsibilitiesGeneral tasks that may sit outside Section 3Include Cross TrainingDeputy Archivist/RPS
Job DemandsThe job may involve the following:Very high concentration of workStrict and tight deadlinesHaving to juggle a range of tasks/issues simultaneouslyWorking in a hazardous environment with high requirement to follow safety proceduresWorking outside normal working hoursNeeding to respond to client demandsThe CandidateTechnical school phlebotomy training or Medical Assistant certificateMinimum two years of active phlebotomy experience preferredRequired to have working knowledge of OSHA regulations and proper blood collection techniques (evaluable during employee orientation period)Company benefitsIn return you will receive a competitive salary, a generous benefits package, excellent training and development, as well as an exciting career within a fast paced and dynamic business.
Company OverviewOur growing and successful business comprises of over 850 talented individuals globally, in an environment where everybody counts and is instrumental to our success. With state-of-the-art manufacturing and clinical facilities in the UK and USA, we deliver a full range of drug development solutions around the globe saving our clients both time and money.People join Quotient Sciences because we are a respected member of the drug development world, specializing in delivering innovative solutions that integrate formulation development, real time GMP manufacturing and clinical testing We pride ourselves on the quality of our services and our engaged culture. We are passionate about helping our customers get new medicines to market.The RoleCollects biological samples, performs phlebotomy, vital signs and ECGs in accordance with the specific activity scheduleTracks overall study event schedule and participant complianceTo ensure study data is collected to a high quality in accordance with Good Clinical Practice (GCP) standardsTo ensure subject safety at all times
Main Tasks and Responsibilities:Responsible for collection of biological samples; e.g. urine, and sputumResponsible for drawing blood specimens (by venipuncture) according to the times specified in the study schedulesResponsible for recording and maintaining records of blood draws and other biological specimen collections (per SOPs) via paper or electronicAssist with the proper labelling and preparation of blood collection tubes when indicatedAssures that all necessary blood collection tubes, equipment and supplies are on the floor prior to blood draw timePrepares the unit for any scheduled activities and upon completion removes all equipment and/or supplies from the floorAble 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 practicePromptly reports any study participants adverse event and/or lack of compliance to the Study Nurse CoordinatorMust be familiar with proper phlebotomy and laboratory procedures in compliance with OSHA regulations, Good Clinical Practices and Quotient Sciences Operating ProceduresResponsible for proper biomedical waste disposal procedures and schedulesResponsible for reading and understanding all protocols and schedulesResponsible for assisting in the recording and distributing of meals to study participants according to strict meal schedulesAssures that the unit is kept clean and orderly at all times and removes any items not permitted from the floorAble to interact and maintain a professional demeanor with study participants during their inpatient stayResponsible for observing confidentiality practices regarding any protocols, subject information and/or any relevant industry information at all timesAssists with the preparation of data collection binders and study documents as assigned by the Study Nurse Coordinator.Assists with any other duties as assignedAdditional Tasks / ResponsibilitiesGeneral tasks that may sit outside Section 3Include Cross TrainingDeputy Archivist/RPS
Job DemandsThe job may involve the following:Very high concentration of workStrict and tight deadlinesHaving to juggle a range of tasks/issues simultaneouslyWorking in a hazardous environment with high requirement to follow safety proceduresWorking outside normal working hoursNeeding to respond to client demandsThe CandidateTechnical school phlebotomy training or Medical Assistant certificateMinimum two years of active phlebotomy experience preferredRequired to have working knowledge of OSHA regulations and proper blood collection techniques (evaluable during employee orientation period)Company benefitsIn return you will receive a competitive salary, a generous benefits package, excellent training and development, as well as an exciting career within a fast paced and dynamic business.