Please note this is a fixed term contract.
As a market leader offering incomparable, industry advancing patient record access via state-of-the-art search and recruit technology, NWEH stand for real discovery. Powered by our network of diverse patient populations, we go further, faster — to deliver true-to-life full service clinical trials. Our ever-growing decentralized tech enabled clinical trials business with industry dominating access to 20 million patient records, attests that we are world leaders in our field. Our model ensures broader, more diverse cohorts to better reflect real-world populations.
At NWEH our focus isn’t just about technology; it’s about reshaping how clinical trials are designed and delivered in the UK and beyond.
Job purpose
As a Research Nurse, you will provide specialist skills and knowledge to support the delivery of clinical research studies. You will liaise with clinical investigators, sponsor companies and external vendors to manage trial protocols. At all times you will be expected to deliver high quality research ensuring participant safety and welfare. The nature of the work is unpredictable, and you will be expected to be flexible and responsive in order to manage various aspects of the job at short notice. You will be expected to participate fully in your own personal development.
Key accountabilities
Key responsibilities include the following:
Responsibilities
* Ensure all research is delivered in accordance with ICH GCP guidelines, including the integrated addendums and the UK Policy Framework for Health and Social Care Research.
* Have familiarity with risk issues pertaining to confidentiality of participant and research related documentation (GDPR and Caldicott Review).
* Ensure compliance with all study protocols and supporting documents.
* Manage multiple studies and sites from set up to closure, including identification and recruitment of patients in accordance with study protocols and agreed targets and timelines.
* Conduct participant screening, eligibility assessment, and provision of information to facilitate effective informed consent or assent.
* Record, report and, where required, escalate adverse drug reactions and adverse events in accordance with study protocol and Clinical Trial Regulations.
* Maintain clear and accurate records and documentation to support all research activity using databases, software and electronic health records, and process and shipment of biological samples.
* Collaborate with data managers and clinical research monitors to ensure timely resolution of data queries.
* Maintain Investigator Site Files and develop and utilise trackers and spreadsheet tools to support study delivery to timelines.
* Participate in audits and inspections as required, and support and execute all activities in line with ISO 9001:2015 and NWEH policies and Standard Operating Procedures.
* Provide effective resource management, mentorship and support for other and new staff members, and support Community Team Leads and management.
* Work in a variety of settings including hospital, community settings, remote and possibly as a lone worker, to meet the demands of studies, promoting research through collaboration and communication with departments within NWEH and external organisations.
* Remain aware of current trends and developments within global clinical research.
* Complete mandatory training, participate in own personal development, identify own learning needs and educational opportunities, working within professional guidelines and in a manner consistent with the Nursing and Midwifery Council code.
Essential Qualifications and Skills
* Registered Nurse NMC Level 1 with effective communication and interpersonal skills and the ability to work flexibly.
* Research experience is essential.
* Ability to explain complex concepts to patients in a clear and concise manner, working autonomously and as a team player.
* Meticulous attention to detail, with a high level of accuracy and demonstrable IT skills.
* Evidence of continuous professional development, high motivation, organisational ability and ability to meet deadlines.
* Valid driving licence, willingness to use own car (mileage recompensed following policy) and insure car for business use.
Desirable Skills
* Knowledge of regulations and governance in clinical research including EU directives and ICH GCP requirements.
* Experience working in Primary Care and Clinical Research.
* Presentation skills, venepuncture proficiency and experience in obtaining informed consent.
* First level degree or studying towards.
Job Types: Full-time, Temporary, Contract
#J-18808-Ljbffr