Quotient Sciences : Molecule to Cure. Fast.
We accelerate drug development by integrating formulation development, clinical testing, data sciences, and manufacturing into one seamless process. Our proprietary platform, Translational Pharmaceutics® , shortens timelines by 9-12 months on average.
Arcinova , our specialist arm in Reading and Alnwick, UK, delivers end-to-end drug substance and early drug product services, including bioanalysis and radiolabeling-streamlining early development from candidate selection to proof of concept.
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 practice
- To collect biological samples, performs phlebotomy, vital signs and ECG's in accordance with the specific activity schedule
- To track overall study event schedule and participant compliance
- To comply and adhere to GCP guidelines and regulations as required of this role
- 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
Main Tasks and Responsibilities
Responsible for the monitoring of volunteer safety as applicable through scope of practiceAble to respond to medical emergency and follow medical directives within scope of practiceResponsible for communicating any noted adverse within scope of practiceAdherence to applicable SOPs and ProtocolResponsible for collection of biological samples; e.g. blood, urine, stool, 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 electronic formsAssist 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 floorMeasures and records vital signs accurately; recognizes and reports any abnormal vital signs accordinglyOperates ECG machine, performs ECGs, and / or works with holter monitors if trained and within scope of practicePromptly reports any study participant's adverse event and / or lack of compliance to the Clinical Research NurseMust 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 demeanour 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 Clinical Research NurseAssists with any other duties as assignedThe Candidate
Current / Valid EMT-Paramedic.Current Advanced Cardiac Life Support (ACLS) certificationMinimum two years of active phlebotomy experience preferredRequired to have working knowledge of OSHA regulations and proper blood collection techniques (evaluable during employee orientation period)Able to follow medical directivesHigh attention to detailsExcellent communication and interpersonal skillsJob Demands
The 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 demandsApplication 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.
Our Commitment to Diversity, Equity and Inclusion
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.
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.
This applies to all aspects of employment, including hiring, promotion, demotion, compensation, training, working conditions, transfer, job assignments, benefits, layoff, and termination.