At a Glance
- Tasks: Deliver clinical research studies and support participants throughout their journey.
- Company: Join a leading clinical research team in Aberdeen, Scotland.
- Benefits: Ongoing professional development, flexible hours, and a collaborative work environment.
- Why this job: Make a real difference in patient care while advancing your nursing career.
- Qualifications: Registered Nurse with GCP knowledge and excellent communication skills.
- Other info: Opportunity to work across multiple clinical areas and gain valuable experience.
The predicted salary is between 36000 - 60000 £ per year.
The Clinical Research Nurse will be responsible for the safe and effective delivery of clinical research studies in accordance with Good Clinical Practice (GCP), regulatory requirements, and local policies. The post holder will work collaboratively with investigators, research teams, and clinical services to support the set-up, conduct, and close-out of clinical trials and research studies.
Key Responsibilities
- Clinical Research Delivery
- Deliver clinical research studies in line with approved protocols, GCP, and ethical approvals
- Screen, recruit, consent, and follow up research participants
- Perform study-related clinical procedures (e.g. observations, venepuncture, ECGs, sample processing)
- Monitor participant safety and report adverse events in accordance with regulatory requirements
- Study Management
- Coordinate study visits and liaise with clinical departments to ensure smooth study delivery
- Maintain accurate and contemporaneous study documentation, including case report forms and source data
- Assist with study set-up, site initiation, monitoring visits, and close-out activities
- Support data collection, query resolution, and audit readiness
- Participant Care and Advocacy
- Act as a patient advocate, ensuring participants are fully informed and supported throughout their research journey
- Provide clear information to participants and respond to questions or concerns
- Ensure confidentiality and data protection standards are upheld at all times
- Collaboration and Communication
- Work closely with Principal Investigators, sponsors, CROs, and multidisciplinary teams
- Communicate effectively with clinical staff, research teams, and external stakeholders
- Contribute to team meetings, service development, and quality improvement initiatives
- Governance and Compliance
- Ensure compliance with GCP, GDPR, MHRA regulations, and local SOPs
- Support inspections and audits as required
- Maintain mandatory training and professional registration
Person Specification
- Registered Nurse (Adult) with valid NMC registration
- Degree-level qualification or equivalent clinical experience
- Knowledge of clinical research and Good Clinical Practice (GCP)
- Excellent communication and interpersonal skills
- Strong organisational skills with attention to detail
- Ability to work independently and as part of a multidisciplinary team
Desirable
- Previous experience in a clinical research or research-active environment
- Valid GCP certification
- Experience in informed consent and clinical trial documentation
- Knowledge of regulatory and ethical frameworks for clinical research
- Experience working with electronic data capture systems
Additional Information
- The post may involve working across multiple clinical areas within Aberdeen
- Some flexibility in working hours may be required to meet study needs
- Ongoing professional development and research training will be supported
Clinical Research Nurse in Aberdeen employer: Barrington James
Contact Detail:
Barrington James Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Nurse in Aberdeen
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field on LinkedIn or at local events. We all know that sometimes it’s not just what you know, but who you know that can help you land that Clinical Research Nurse role.
✨Tip Number 2
Prepare for interviews by brushing up on your GCP knowledge and understanding of clinical trials. We recommend practising common interview questions with a friend or mentor to boost your confidence and show off your expertise.
✨Tip Number 3
Don’t forget to showcase your patient advocacy skills! During interviews, share examples of how you’ve supported participants in previous roles. This will highlight your commitment to participant care, which is crucial for a Clinical Research Nurse.
✨Tip Number 4
Apply through our website! We make it easy for you to find and apply for roles that match your skills. Plus, it shows us you’re genuinely interested in joining our team and contributing to impactful clinical research.
We think you need these skills to ace Clinical Research Nurse in Aberdeen
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that match the Clinical Research Nurse role. Highlight your nursing qualifications, any clinical research experience, and your understanding of GCP. We want to see how you fit into our team!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical research and how your background makes you a great fit for us. Be sure to mention specific experiences that relate to the job description.
Showcase Your Communication Skills: As a Clinical Research Nurse, communication is key. In your application, demonstrate your ability to communicate effectively with both participants and team members. This could be through examples of past experiences or projects you've worked on.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen to join our team at StudySmarter!
How to prepare for a job interview at Barrington James
✨Know Your GCP Inside Out
As a Clinical Research Nurse, understanding Good Clinical Practice (GCP) is crucial. Brush up on the key principles and be ready to discuss how you've applied them in your previous roles. This shows you’re not just familiar with the guidelines but can also implement them effectively.
✨Showcase Your Communication Skills
Effective communication is key in this role. Prepare examples of how you've communicated complex information to participants or collaborated with multidisciplinary teams. Highlighting your interpersonal skills will demonstrate that you can advocate for patients and work well with others.
✨Be Ready for Scenario Questions
Expect scenario-based questions that assess your problem-solving abilities and ethical considerations. Think about past experiences where you had to make quick decisions regarding participant safety or compliance with regulations, and be prepared to share those stories.
✨Demonstrate Your Organisational Skills
The role requires strong organisational skills, so come prepared to discuss how you manage multiple tasks and maintain accurate documentation. Share specific strategies you use to stay organised, especially when coordinating study visits or managing participant data.