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- Tasks: Monitor clinical trials, manage study protocols, and ensure compliance with regulations.
- Company: Leading clinical research organisation in Reading with a focus on innovation.
- Benefits: Gain valuable experience in the clinical research field with potential for career advancement.
- Other info: Flexibility to travel and direct communication with study sites is essential.
- Why this job: Make a difference in healthcare by ensuring studies run smoothly and ethically.
- Qualifications: Life science degree or equivalent experience; knowledge of Good Clinical Practice required.
The predicted salary is between 30000 - 40000 £ per year.
A leading clinical research organization in Reading is seeking junior and experienced Clinical Research Associates to perform monitoring visits, manage study protocols, and ensure compliance with regulatory standards.
Candidates should have a life science degree or equivalent experience, along with knowledge of Good Clinical Practice and ICH guidelines.
This role involves direct communication with study sites and requires flexibility to travel.
Note that this position does not offer UK visa sponsorship.
Clinical Research Associate II – Site Monitoring & Trials employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate II – Site Monitoring & Trials
✨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 valuable personal connections can be in landing that dream job.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of Good Clinical Practice and ICH guidelines. We recommend practising common interview questions with a friend to boost your confidence and show off your expertise.
✨Tip Number 3
Don’t just apply anywhere; focus on organisations that align with your values and career goals. We suggest checking out our website for tailored opportunities that fit your skills and interests.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can set you apart from other candidates. We believe it shows your enthusiasm and professionalism, which are key in the clinical research world.
We think you need these skills to ace Clinical Research Associate II – Site Monitoring & Trials
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in clinical research. We want to see how your background aligns with the role, so don’t be shy about showcasing your life science degree and any previous monitoring visits you've conducted.
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 you can contribute to our team. We love seeing candidates who are genuinely excited about the role and the impact they can make.
Showcase Your Knowledge: Familiarise yourself with Good Clinical Practice and ICH guidelines, and mention them in your application. We appreciate candidates who understand the regulatory landscape and can demonstrate their knowledge in this area.
Apply Through Our Website: We encourage you to apply directly through our website for a smoother process. It helps us keep track of applications and ensures you’re considered for the role without any hiccups!
How to prepare for a job interview at IQVIA
✨Know Your Stuff
Make sure you brush up on your knowledge of Good Clinical Practice and ICH guidelines. Being able to discuss these topics confidently will show that you’re serious about the role and understand the industry standards.
✨Showcase Your Experience
Prepare specific examples from your past experiences where you've successfully managed study protocols or conducted monitoring visits. This will help demonstrate your practical skills and how they align with what the organisation is looking for.
✨Be Ready to Discuss Travel Flexibility
Since the role requires travel, be prepared to talk about your availability and willingness to travel for site visits. Highlight any previous experiences where you’ve had to adapt to travel demands in your work.
✨Engage with Questions
At the end of the interview, don’t forget to ask insightful questions about the company’s current trials or their approach to compliance. This shows your genuine interest in the role and helps you assess if it’s the right fit for you.