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 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 Reading employer: High5
Join a forward-thinking organisation in Reading, where as a Clinical Research Associate, you will be part of a dynamic team dedicated to advancing Oncology studies. We pride ourselves on fostering a collaborative work culture that prioritises employee growth and continuous learning, offering comprehensive training and development opportunities. With a commitment to making a meaningful impact in the healthcare sector, we provide a supportive environment that values innovation and excellence.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate in Reading
✨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
Prepare for interviews by brushing up on your knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. We recommend practising common interview questions related to site monitoring and study management to show you’re ready to hit the ground running.
✨Tip Number 3
Showcase your flexibility and willingness to travel! In your conversations with potential employers, highlight your readiness to visit sites across the UK. This can set you apart from other candidates who may not be as open to travel.
✨Tip Number 4
Don’t forget to apply through our website! We’ve got loads of resources to help you land that Clinical Research Associate role. Plus, applying directly shows your enthusiasm and commitment to joining our team.
We think you need these skills to ace Clinical Research Associate in Reading
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 candidates who can ensure quality and integrity in their work.
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 don’t miss out on any important updates from 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 interested in making an impact.
✨Demonstrate Your Monitoring Skills
Be prepared to discuss your experience with site monitoring visits. Think of specific examples where you've successfully managed recruitment plans or resolved issues at sites. Highlight your ability to adapt and communicate effectively with site staff, as this is crucial for the role.
✨Showcase Your Organisational Skills
As a Clinical Research Associate, you'll need to juggle multiple tasks. Bring examples of how you've tracked regulatory submissions, managed documentation, or maintained trial master files in previous roles. This will demonstrate your attention to detail and organisational prowess.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's approach to clinical trials and their expectations for the role. This not only shows your interest but also gives you a chance to assess if the company aligns with your career goals. Remember, interviews are a two-way street!
