At a Glance
- Tasks: Monitor clinical sites and ensure compliance with study protocols in Oncology research.
- Company: Join a leading clinical research organisation making a real impact in healthcare.
- Benefits: Full-time role with opportunities for travel, professional growth, and continuous learning.
- Other info: Dynamic role with a focus on collaboration and career advancement.
- Why this job: Be part of groundbreaking research that shapes the future of cancer treatment.
- Qualifications: Experience in Oncology monitoring and knowledge of GCP and ICH guidelines required.
The predicted salary is between 35000 - 45000 £ per year.
The Clinical Research Associate will support Oncology studies and cover sites across the UK. Apply today and forge a career with greater purpose, make an impact and never stop learning!
Responsibilities
- 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. May support start-up phase.
- 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.
Requirements
- Experience of independent on-site monitoring of Oncology therapeutic area for unblinded studies.
- In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Life science degree educated or equivalent industry experience.
- Flexibility to travel to sites as required.
Clinical Research Associate in Brighton employer: SLAMcore
Join a dynamic team in Brighton, where your role as a Clinical Research Associate will not only contribute to groundbreaking Oncology studies but also foster a culture of continuous learning and professional growth. With a commitment to excellence and adherence to Good Clinical Practice, we offer a supportive work environment that values collaboration and innovation, ensuring you make a meaningful impact in the field of clinical research.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate in Brighton
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field, especially those working in oncology. Attend industry events or webinars, and don’t be shy about asking for informational interviews – it’s all about making connections that could lead to your next opportunity.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. We recommend creating a list of common interview questions for Clinical Research Associates and practising your responses to show you’re ready to hit the ground running.
✨Tip Number 3
Showcase your flexibility and willingness to travel! Since this role involves site monitoring across the UK, make sure to highlight any previous experience you have with travel or managing multiple sites. It’s all about demonstrating that you can adapt to the demands of the job.
✨Tip Number 4
Don’t forget to apply through our website! We’ve got a streamlined application process that makes it easy for you to showcase your skills and experience. Plus, it shows us you’re genuinely interested in joining our team at StudySmarter!
We think you need these skills to ace Clinical Research Associate in Brighton
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Research Associate role. Highlight your experience in Oncology studies and any relevant skills that match the job description. We want to see how you can make an impact!
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 aligns with our mission at StudySmarter. Keep it engaging and personal.
Showcase Your GCP Knowledge:Since Good Clinical Practice is key for this role, make sure to mention your understanding of GCP and ICH guidelines. We’re looking for someone who knows their stuff and can ensure quality and integrity in study practices.
Apply Through Our Website:Don’t forget to apply through our website! It’s the best way for us to receive your application and keep track of all the amazing candidates. Plus, it shows you’re keen on joining our team!
How to prepare for a job interview at SLAMcore
✨Know Your Oncology Stuff
Make sure you brush up on your knowledge of oncology studies and the specific challenges they present. Familiarise yourself with recent advancements in the field, as well as any relevant GCP and ICH guidelines. This will show that you're not just interested in the role, but that you’re genuinely passionate about making an impact in clinical research.
✨Demonstrate Your Monitoring Skills
Be prepared to discuss your experience with site monitoring visits. Think of specific examples where you've successfully managed site communications or resolved issues. Highlight your ability to adapt recruitment plans and ensure compliance with protocols, as this is crucial for the role.
✨Showcase Your Team Spirit
Collaboration is key in clinical research. Be ready to talk about how you've worked with study teams in the past. Share instances where you’ve liaised effectively with team members to support project execution. This will demonstrate your ability to work well within a team and contribute positively to the study’s success.
✨Ask Insightful Questions
Prepare some thoughtful questions to ask at the end of your interview. Inquire about the company’s approach to site management or how they handle challenges in subject recruitment. This shows that you’re engaged and thinking critically about the role, which can leave a lasting impression on the interviewers.
