At a Glance
- Tasks: Monitor clinical sites and ensure compliance with study protocols in oncology research.
- Company: Join a leading team dedicated to creating a healthier world through innovative research.
- Benefits: Full-time role with opportunities for travel, professional growth, and impactful work.
- Other info: Dynamic field-based role with a focus on continuous learning and collaboration.
- Why this job: Make a real difference in healthcare while advancing your career in clinical research.
- Qualifications: Experience in oncology monitoring and knowledge of GCP and ICH guidelines required.
The predicted salary is between 35000 - 45000 € per year.
Reading, United Kingdom | Full time | Field-based
IQVIA's Site Management (multi-sponsor) team are seeking a Clinical Research Associate to join us on our mission to help create a healthier world. 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.
- 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.
*Please note - this role is not eligible for visa sponsorship*
Clinical Research Associate in Reading employer: IQVIA Argentina
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation in the field of clinical research. Our Clinical Research Associates enjoy comprehensive benefits, ongoing professional development opportunities, and the chance to make a meaningful impact on global health, all while working in the vibrant setting of Reading, UK. Join us to advance your career in a supportive environment where your contributions truly matter.
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 on LinkedIn or at industry events. We can’t stress enough how personal connections can lead to job opportunities that aren’t even advertised.
✨Tip Number 2
Prepare for interviews by researching the company and its projects. We recommend practising common interview questions and tailoring your answers to highlight your experience in Oncology studies. Show them you’re the perfect fit!
✨Tip Number 3
Follow up after interviews! A quick thank-you email can set you apart from other candidates. We suggest mentioning something specific from your conversation to remind them of your enthusiasm and fit for the role.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, we love seeing candidates who are proactive about their job search. Let’s get you started on this exciting journey!
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 someone who knows their stuff and can ensure quality in site management.
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 serious about joining our team!
How to prepare for a job interview at IQVIA Argentina
✨Know Your Oncology Stuff
Make sure you brush up on your knowledge of Oncology studies and the specific challenges they face. Being able to discuss recent advancements or common issues in this field will show that you're not just familiar with the role, but genuinely interested in making an impact.
✨Master Good Clinical Practice (GCP)
Since GCP is a big part of the job, ensure you can talk confidently about its principles and how they apply to site monitoring. Prepare examples from your past experiences where you adhered to these guidelines, as it’ll demonstrate your commitment to quality and compliance.
✨Show Your Communication Skills
As a Clinical Research Associate, you'll need to liaise with various stakeholders. Think of examples where you've successfully communicated complex information or resolved conflicts. This will highlight your ability to manage ongoing project expectations and maintain strong relationships with sites.
✨Be Ready to Discuss Problem-Solving
Prepare to share instances where you've encountered challenges in previous roles and how you tackled them. Whether it's about recruitment issues or regulatory hurdles, showcasing your problem-solving skills will reassure the interviewers that you can handle the dynamic nature of clinical research.
