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 difference in healthcare.
- Benefits: Full-time role with opportunities for travel, professional growth, and impactful work.
- Other info: Dynamic role with a focus on continuous learning and collaboration.
- Why this job: Make a meaningful impact in cancer research while developing your career.
- Qualifications: Experience in oncology monitoring and knowledge of GCP and ICH guidelines.
The predicted salary is between 37000 - 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 Chesterfield employer: High5
Join a forward-thinking organisation in Chesterfield that prioritises employee development and fosters a collaborative work culture. As a Clinical Research Associate, you will not only contribute to impactful Oncology studies but also benefit from ongoing training and career advancement opportunities in a supportive environment. With a commitment to excellence and innovation, this company stands out as an exceptional employer for those seeking meaningful and rewarding careers in clinical research.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate in Chesterfield
✨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 job fair or through networking, be ready to discuss your experience with site monitoring and GCP. Bring along examples of your work or even a portfolio to demonstrate your expertise.
✨Tip Number 3
Follow up after interviews! A quick thank-you email can go a long way. Mention something specific from your conversation to remind them of your fit for the Clinical Research Associate role. It shows your enthusiasm and keeps you on their radar.
✨Tip Number 4
Don’t forget to apply through our website! We’ve got loads of opportunities waiting for you, and applying directly can sometimes give you an edge. Plus, it’s super easy to keep track of your applications and updates!
We think you need these skills to ace Clinical Research Associate in Chesterfield
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 in our studies.
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. Let’s get started on this journey together!
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 manage multiple studies and ensure all documentation is in order. Bring examples of how you've kept track of regulatory submissions, CRF completions, and other essential paperwork in previous roles. This will demonstrate your attention to detail and organisational prowess.
✨Ask Insightful Questions
At the end of the interview, don’t shy away from asking questions about the company’s approach to clinical trials or their expectations for the role. This shows that you're engaged and thinking critically about how you can contribute to their success. Plus, it gives you a chance to assess if the company is the right fit for you!
