Research Nurse
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Job Summary
What can we offer you
Apart from job satisfaction we can offer you:
YOURSELF
25 days holiday (with the option to buy more)
HEALTH
Private Healthcare
Optional dental insurance health assessments and health cash plans
Cycle to Work scheme
WEALTH
Company Pension Scheme matching contributions up to 5% of salary
Life assurance
Annual staff bonus scheme
Season ticket loans
Job Purpose
Working in our state-of-the-artClinical Trial Imaging Clinic in West London as Research Nurse (Study Coordinator) your role will be to provide care to our clinical study participants (patients) and coordinate the clinical support activities vital to the safe completion of the procedures involved in our Imaging and Experimental Medicine studies.
Reporting to the Principal Study Coordinator within a small supportive team forming part of our Clinical Operations group this is a highly patient-centric role. Your work will be divided between hands-on participant-contact work (welcoming & explaining procedures / providing reassurance conducting pre-clinical assessments administering specified drugs inserting cannulas taking blood samples etc.) coordinating logistics and set-up activities (planning necessary assessments scheduling appointments etc.) and ensuring the timely completion of all related documentation for the studies to which youre assigned in compliance with current regulatory requirements.
The safety of our participants is of paramount importance to us. Reflecting this your focus will be on making sure that they feel - at all times - informed comfortable and supported.
Key Responsibilities
Participant Safety and Wellbeing (approximately 50% of the time)
Ensure participant safety and wellbeing.
Perform safety assessments in accordance with protocol and GCP.
Maintain visible presence during participant visits.
Maintain ILS-level emergency response competency.
Maintain nursing professional accreditation and CPD.
Study Management
Manage assigned portfolio of studies prioritizing tasks to meet timelines.
Review new study protocols and provide feedback.
Implement protocol amendments promptly.
Report deviations from SOPs protocol or GCP to management.
Study Conduct
Conduct and manage research studies in accordance with approved protocols SOPs and ICH-GCP.
Ensure data integrity and compliance with ethical standards.
Maintain competence in technical equipment and procedures.
Ensure training and competency records are current.
Quality Management
Perform QC of essential documents and study data.
Host monitoring visits and ensure compliance.
Assist in SOP review and implementation.
Conduct change controls and self-audits on a timely basis.
Laboratory Work
Perform study-related lab duties including sample processing storage and dispatch per regulations.
Maintain compliance with regulations governing HBSM.
Teamwork
Collaborate effectively with internal and external stakeholders.
Support team initiatives and share best practices.
Other
Perform necessary administrative and IT- related tasks.
Perform routine housekeeping and cleaning duties as needed.
Work with radiation and adhere to safety precautions.
Amenable to flexible working pattern to cover scans schedule and schedule adjustments.
Functional Competencies (Technical knowledge/Skills)
Able to demonstrate empathy sensitivity and a willingness to go out of ones way to ensure a high standard of care is maintained.
Willingness to work hands on supporting other team members with more basic ancillary tasks and in maintaining good housekeeping.
Knowledge of clinical research processes and ICH-GCP standards.
Sound interpersonal verbal and written communication skills.
Ability to manage multiple tasks prioritize effectively and maintain attention to detail.
Proficiency in electronic data capture systems and clinical software tools ideally.
Flexible and proactive approach to work assignments and process improvements.
Competence in the use of technical equipment and laboratory procedures.
Ability to work collaboratively in a multidisciplinary and global team environment.
Experience Education and Certifications
Registered General Nurse (RGN) with current NMC registration.
Nursing experience (acute medicine neurology experience advantageous but not essential).
Previous experience in clinical research and an understanding of drug development processes would be a significant advantage.
Resuscitation training to ILS level; competent in emergency equipment use.
Computer literate with proficiency in electronic data capture systems.
Practical Considerations
Working hours: Monday to Friday 8am to 4pm with flexibility to start slightly earlier and work later when required preferred.
Complimentary allocated parking provided on-site
Required Experience:
IC
Key Skills
- Clinical Research
- FDA Regulations
- Data Collection
- GCP
- Infusion Experience
- Phlebotomy
- Clinical Trials
- Pediatrics Experience
- Qualitative Research Interviewing
- Research Experience
- Nursing
- Epic
About Company
Interactive Response Technology or IRT is used in clinical trials. But what is IRT? Find out more about how Perceptive eClinical's IRT system
