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 practiceÂ
- To collect biological samples, performs phlebotomy, vital signs and ECG’s in accordance with the specific activity scheduleÂ
- To track overall study event schedule and participant complianceÂ
- To comply and adhere to GCP guidelines and regulations as required of this roleÂ
- To ensure study data is collected to a high quality in accordance with Good Clinical Practice (GCP) standardsÂ
- To ensure subject safety at all timesÂ
Main Tasks and Responsibilities
- Responsible for the monitoring of volunteer safety as applicable through scope of practiceÂ
- Able to respond to medical emergency and follow medical directives within scope of practiceÂ
- Responsible for communicating any noted adverse within scope of practiceÂ
- Adherence to applicable SOPs and ProtocolÂ
- Responsible for collection of biological samples; e.g. blood, urine, stool, sputumÂ
- Responsible for drawing blood specimens (by venipuncture) according to the times specified in the study schedulesÂ
- Responsible for recording and maintaining records of blood draws and other biological specimen collections (per SOPs) via paper or electronic formsÂ
- Assist with the proper labelling and preparation of blood collection tubes when indicatedÂ
- Assures that all necessary blood collection tubes, equipment and supplies are on the floor prior to blood draw timeÂ
- Prepares the unit for any scheduled activities and upon completion removes all equipment and/or supplies from the floorÂ
- Measures and records vital signs accurately; recognizes and reports any abnormal vital signs accordinglyÂ
- Operates ECG machine, performs ECGs, and/or works with holter monitors if trained and within scope of practiceÂ
- Promptly reports any study participant’s adverse event and/or lack of compliance to the Clinical Research NurseÂ
- Must be familiar with proper phlebotomy and laboratory procedures in compliance with OSHA regulations, Good Clinical Practices and Quotient Sciences Operating ProceduresÂ
- Responsible for proper biomedical waste disposal procedures and schedulesÂ
- Responsible for reading and understanding all protocols and schedulesÂ
- Responsible for assisting in the recording and distributing of meals to study participants according to strict meal schedulesÂ
- Assures that the unit is kept clean and orderly at all times and removes any items not permitted from the floorÂ
- Able to interact and maintain a professional demeanour with study participants during their inpatient stayÂ
- Responsible for observing confidentiality practices regarding any protocols, subject information and/or any relevant industry information at all timesÂ
- Assists with the preparation of data collection binders and study documents as assigned by the Clinical Research NurseÂ
- Assists with any other duties as assignedÂ
Job DemandsÂ
The job may involve the following:Â
- Very high concentration of workÂ
- Strict and tight deadlinesÂ
- Having to juggle a range of tasks/issues simultaneouslyÂ
- Working in a hazardous environment with high requirement to follow safety proceduresÂ
- Working outside normal working hoursÂ
- Needing to respond to client demandsÂ
The Candidate
- Current/Valid EMT-Basic or EMT-Paramedic. If Paramedic current Advanced Cardiac Life Support (ACLS) certificationÂ
- Minimum two years of active phlebotomy experience preferredÂ
- Required to have working knowledge of OSHA regulations and proper blood collection techniques (evaluable during employee orientation period)Â
- Able to follow medical directivesÂ
- High attention to detailsÂ
- Excellent communication and interpersonal skillsÂ
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#INDHP
Application Requirements
When applying for a position with Quotient Sciences to be able to work in our organization you must be aged 18 years or over and not have been debarred by the FDA. If you indicate you are under the age of 18 or have been debarred then your application will be automatically declined.Â
Our Commitment to Diversity, Equity and InclusionÂ
Quotient Sciences are advocates for positive change and conscious inclusion. We strive to create a diverse Quotient workforce and develop a workplace culture that provides a sense of acceptance for every person within our organization. As a global employer, we recognize the value in having an organization that is a true reflection and representation of our society today.Â
Specifically we will not discriminate on the basis of race, color, creed, religion, gender, gender identity, pregnancy, marital status, partnership status, domestic violence victim status, sexual orientation, age, national origin, alienage or citizenship status, veteran or military status, disability, medical condition, genetic information, caregiver status, unemployment status or any other characteristic prohibited by federal, state and/or local laws.Â
This applies to all aspects of employment, including hiring, promotion, demotion, compensation, training, working conditions, transfer, job assignments, benefits, layoff, and termination.
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