At a Glance
- Tasks: Support Oncology studies by monitoring sites and ensuring compliance with regulations.
- Company: Leading clinical research organisation based in Brighton, UK.
- Benefits: Full-time role with opportunities for travel and professional growth.
- Other info: Dynamic role with a focus on collaboration and communication.
- Why this job: Make a difference in cancer research while gaining hands-on experience.
- Qualifications: Life science degree or equivalent experience; independent monitoring skills required.
The predicted salary is between 30000 - 40000 € per year.
The Clinical Research Associate will support Oncology studies and cover sites across the UK.
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
- Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.
- Escalate quality issues as appropriate.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.
- Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
- Collaborate and liaise with study team members for project execution support as appropriate.
- Experience of independent on-site monitoring of Oncology therapeutic area for unblinded studies.
- Life science degree educated or equivalent industry experience.
- Flexibility to travel to sites as required.
Research Associate in Brighton employer: High5
As a leading employer in the clinical research field, we offer our Research Associates a dynamic work environment in Brighton, where collaboration and innovation thrive. Our commitment to employee growth is evident through comprehensive training programmes and opportunities for career advancement, all while fostering a supportive culture that values work-life balance and community engagement. Join us to make a meaningful impact in Oncology studies and be part of a team dedicated to excellence in clinical research.
StudySmarter Expert Advice🤫
We think this is how you could land Research Associate in Brighton
✨Tip Number 1
Networking is key! Reach out to professionals in the oncology field on LinkedIn or at industry events. We can help you connect with others who might know about job openings or can give you insider tips.
✨Tip Number 2
Prepare for interviews by practising common questions related to clinical research and oncology. We suggest doing mock interviews with friends or using online resources to boost your confidence and refine your answers.
✨Tip Number 3
Showcase your skills! Create a portfolio that highlights your experience in site monitoring and project management. We recommend including any relevant case studies or examples of your work to impress potential employers.
✨Tip Number 4
Don’t forget to apply through our website! We regularly update our job listings, and applying directly can sometimes give you an edge. Plus, it’s super easy to keep track of your applications this way!
We think you need these skills to ace Research Associate in Brighton
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Research Associate role. Highlight any relevant experience in clinical research, especially in Oncology, and showcase your skills in site monitoring and project management.
Craft a Compelling Cover Letter:Your cover letter should tell us why you're the perfect fit for this position. Share your passion for clinical research and how your background aligns with our needs. Don't forget to mention your flexibility to travel!
Showcase Your Communication Skills:Since you'll be liaising with various sites, it's crucial to demonstrate your strong communication skills. Use examples from your past experiences where you effectively managed expectations or resolved issues.
Apply Through Our Website:We encourage you to apply directly through our website. This way, we can easily track your application and ensure it gets the attention it deserves. Plus, it shows you're keen on joining our team!
How to prepare for a job interview at High5
✨Know Your Oncology Stuff
Make sure you brush up on your knowledge of oncology studies and the specific protocols related to them. Familiarise yourself with Good Clinical Practice (GCP) guidelines, as well as any recent developments in the field. This will show that you're not just interested in the role but also passionate about the subject matter.
✨Demonstrate Your Monitoring Skills
Be prepared to discuss your experience with site monitoring visits. Think of specific examples where you've successfully managed site selection, initiation, or close-out visits. Highlight how you’ve handled challenges in previous roles, especially regarding recruitment plans and maintaining communication with sites.
✨Showcase Your Organisational Skills
As a Research Associate, you'll need to manage multiple tasks simultaneously. Bring examples of how you've tracked regulatory submissions, monitored study progress, or maintained documentation in the past. This will help illustrate your ability to keep everything organised and compliant with regulations.
✨Ask Insightful Questions
Prepare some thoughtful questions to ask during the interview. Inquire about the team dynamics, the specific challenges they face in their oncology studies, or how they measure success in this role. This shows that you're engaged and genuinely interested in contributing to their projects.
