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, learning, and career growth.
- Other info: Dynamic work environment with a focus on continuous learning and professional development.
- Why this job: Make a difference in patients' lives while advancing your career in clinical research.
- Qualifications: Experience in Oncology monitoring and knowledge of GCP and ICH guidelines.
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: High5
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 collaboration, we offer a supportive work environment that values your contributions and encourages you to 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 job opportunities.
✨Tip Number 2
Show off your skills! When you get the chance to meet potential employers, whether at a networking event or an interview, be ready to discuss your experience with site monitoring and GCP. Use specific examples to demonstrate how you've tackled challenges in previous roles.
✨Tip Number 3
Stay proactive! If you see a job opening that excites you, apply through our website and follow up with a friendly email. This shows your enthusiasm and keeps you on their radar. Plus, it’s a great way to express your interest in the role directly!
✨Tip Number 4
Prepare for the unexpected! Interviews can throw curveballs, so brush up on your knowledge of ICH guidelines and be ready to discuss how you would handle various scenarios in site management. Confidence is key, so practice makes perfect!
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, be sure to mention your understanding of GCP and ICH guidelines. We’re looking for someone who knows their stuff and can ensure quality in our studies.
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 High5
✨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 a candidate, but someone who is genuinely passionate about the area.
✨Demonstrate Your Monitoring Skills
Prepare to discuss your experience with site monitoring visits. Think of specific examples where you've successfully managed site relationships or resolved issues. Being able to articulate your approach to monitoring and how you ensure compliance will set you apart from other candidates.
✨Show Your Communication Prowess
As a Clinical Research Associate, communication is key. Be ready to share examples of how you've established effective lines of communication with study sites. Highlight your ability to adapt your communication style to different stakeholders, ensuring everyone is on the same page throughout the project.
✨Be Ready for Travel Talk
Since the role requires flexibility to travel, be prepared to discuss your availability and willingness to visit various sites across the UK. It’s a good idea to mention any previous travel experiences related to work, showcasing your adaptability and commitment to the role.
