At a Glance
- Tasks: Monitor clinical trial sites and ensure compliance with regulations while supporting innovative research.
- Company: Join IQVIA, a top-rated company in healthcare innovation and research.
- Benefits: World-class training, career development, and the chance to work on cutting-edge medicines.
- Other info: Flexible travel opportunities and a commitment to integrity in hiring.
- Why this job: Make a real impact in healthcare and grow your career in a dynamic environment.
- Qualifications: 18 months of monitoring experience and a life science degree or equivalent.
The predicted salary is between 35000 - 45000 € per year.
Join Us on Our Mission to Drive Healthcare Forward. IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK. With access to world-class training and professional development, we’ll give you the tools you need to create the career you want.
Why IQVIA? IQVIA is recognized as #1 in its category on the 2026 Fortune® World’s Most Admired Companies™ list for the fifth consecutive year! We offer genuine career development opportunities for those who want to grow as part of the organization. The chance to work on cutting edge medicines at the forefront of new medicines development. IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!
Responsibilities
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- 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
- A minimum of 18 months of independent on-site monitoring.
- You have successfully managed multiple clinical trial protocols across diverse investigative sites.
- 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.
Apply today and forge a career with greater purpose, make an impact, and never stop learning!
*Please note - this role is not eligible for UK visa sponsorship.*
Research Associate – Oncology in Bracknell employer: IQVIA
At IQVIA, we are dedicated to driving healthcare forward, offering our Research Associates unparalleled access to world-class training and professional development opportunities. Our collaborative work culture fosters innovation and growth, allowing you to contribute to cutting-edge medicines while enjoying the benefits of a supportive environment that prioritises your career advancement. Join us in making a meaningful impact on patient outcomes and experience the unique advantages of working with a globally recognised leader in clinical research.
StudySmarter Expert Advice🤫
We think this is how you could land Research Associate – Oncology in Bracknell
✨Network Like a Pro
Get out there and connect with people in the industry! Attend conferences, webinars, or local meetups related to oncology and clinical research. You never know who might have a lead on your dream job!
✨Show Off Your Skills
When you get the chance to chat with potential employers, make sure to highlight your experience with GCP and ICH guidelines. Share specific examples of how you've successfully managed clinical trials – this will set you apart from the crowd!
✨Follow Up After Interviews
Don’t just sit back after an interview! Send a quick thank-you email to express your appreciation for the opportunity. It shows you're genuinely interested and keeps you fresh in their minds.
✨Apply Through Our Website
Make sure to apply directly through our website for the best chance at landing that Research Associate role. We love seeing candidates who are proactive and take the initiative to connect with us directly!
We think you need these skills to ace Research Associate – Oncology in Bracknell
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Research Associate role. Highlight your experience in clinical trials and any relevant skills that match the job description. We want to see how you can contribute to our mission!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about oncology and how your background makes you a great fit for IQVIA. Let us know what drives you in this field!
Showcase Your Experience:When detailing your experience, focus on specific examples of site monitoring and protocol management. We love seeing concrete achievements that demonstrate your ability to handle the responsibilities outlined in the job description.
Apply Through Our Website:Don’t forget to apply through our website! It’s the best way to ensure your application gets the attention it deserves. Plus, we’re excited to see your application come through directly!
How to prepare for a job interview at IQVIA
✨Know Your GCP and ICH Guidelines
Make sure you brush up on Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines before your interview. Being able to discuss these in detail will show that you’re not just familiar with them, but that you understand their importance in clinical research.
✨Showcase Your Monitoring Experience
Prepare specific examples from your past experience where you successfully managed multiple clinical trial protocols. Highlight any challenges you faced and how you overcame them, as this will demonstrate your problem-solving skills and adaptability.
✨Understand the Role of Site Management
Familiarise yourself with the responsibilities of site monitoring visits, including selection, initiation, and close-out visits. Be ready to discuss how you would handle communication with sites and manage ongoing project expectations effectively.
✨Express Your Passion for Healthcare
IQVIA is all about driving healthcare forward, so make sure to convey your passion for the industry during the interview. Share why you want to work in oncology and how you see yourself contributing to the development of cutting-edge medicines.
