Clinical Research Nurse

at  Quotient Sciences

Quotient Sciences is a drug development and manufacturing accelerator providing integrated programs and tailored services across the entire development pathway. Cutting through silos across a range of drug development capabilities, we help biotech and pharma customers save precious time and money in getting drugs to patients.
We employ more than 1,100 talented individuals globally, located at state-of-the-art development, manufacturing and clinical facilities in the UK and USA. Science, Agility and Culture are the core components that define Quotient Sciences, enabling us to do what we do in the way that we do it.
People join Quotient Sciences because we are a respected member of the drug development community that’s focused on innovation and are driven by an unswerving belief that ideas need to become solutions, and molecules need to become cures, fast. Because humanity needs solutions, fast.
The Role
This is a fantastic opportunity for a Registered Nurse looking to take the next step in their career in clinical research. You will work on a wide range of leading clinical trials with a multifunctional team, broadening your skills and helping pharmaceutical companies progress new medicines to market. The position will be clinic based at our Nottingham site and our facility is made up of 85 beds across 6 wards which has recently undergone extensive refurbishment and operates 24 hours a day, 7 days a week.
This is a fulltime and permanent role with flexible opportunities available.
We also offer free and secure onsite parking.
We are interested in hearing from registered nurses or graduate nurses looking for a role next year.
The Candidate
No prior clinical research experience is required, a full training programme is provided.
We pride ourselves on being a dynamic and supportive company offering full training and career progression opportunities. Immediate Life Support training will also be provided.

• Ensure that the dignity, health, safety, and welfare of study participants is the highest priority at all times
• Perform study related procedures such as cannulation, venepuncture, telemetry, holters, vital signs, ECGs, collection of blood samples., in accordance with ICH-GCP
• Utilise nursing assessment skills to support general well-being of study participants and potential adverse events. Document adverse events and take appropriate action as needed including administration of concomitant medications
• Utilise your skills, knowledge and clinical judgement to assess vital signs
• Provide a lead role in responding to emergency situations. Participate in training scenarios and support the Training and Compliance Team with ILS training of non-clinical staff.
• Use prior clinical experience and knowledge to assist clinical leads and deputies with the preparation of clinical trials.
• Review, check and maintain compliance of emergency equipment in line with phase 1 accreditation scheme requirements.
• Administration of dosage forms inclusive of various routes and devices in accordance with the study specific protocol
• To record data obtained in a timely manner according to the protocol
• Support the clinical team to ensure that source data completion is to a high standard
• Quality control checking of eSource and paper source documents
• To obtain Nurse Led Informed Consent by educating, explaining and informing participants of study procedures in conjunction with ICF.
• Monitor compliance within the clinical unit and support audit readiness at all times
• Lead by example to encourage professional conduct and ensure clinical excellence is maintained across the clinic.
• Support activities in other departments as deemed necessary to support the needs of the business
• Monitor and enforce good infection control practices and provide infection control training for all clinic staff
• Assist senior nursing staff with hepatitis b staff vaccination programme
• Support training and mentorship for both new and existing members of the clinic team