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- Tasks: Monitor clinical sites and ensure compliance with study protocols and regulations.
- Company: Global leader in clinical research with a commitment to excellence.
- Benefits: Competitive salary, professional development, and a dynamic work environment.
- Why this job: Join a team making a real difference in healthcare through innovative research.
- Qualifications: Bachelor's degree and at least one year of on-site monitoring experience required.
- Other info: Based in Livingston, Scotland; no UK visa sponsorship available.
The predicted salary is between 36000 - 60000 £ per year.
A global leader in clinical research is seeking an experienced Clinical Research Associate to ensure sites conduct studies in compliance with protocols and regulations. This role involves performing site monitoring visits, managing study progress, and ensuring documentation is filed correctly.
Candidates should have a Bachelor's degree and at least a year of on-site monitoring experience. Strong communication skills and proficiency with Microsoft Office are required.
The position is based in Livingston, Scotland and does not offer UK visa sponsorship.
Senior Clinical Research Associate: Single Sponsor (UK) in Livingston employer: IQVIA LLC
Contact Detail:
IQVIA LLC Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Research Associate: Single Sponsor (UK) in Livingston
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field. Attend industry events or webinars, and don’t be shy about asking for introductions. We all know someone who knows someone, and that could be your ticket to landing that Senior Clinical Research Associate role!
✨Tip Number 2
Prepare for those interviews! Research the company and its recent studies. Be ready to discuss how your experience aligns with their needs, especially around site monitoring and compliance. We want you to shine, so practice common interview questions and have your own ready to go!
✨Tip Number 3
Show off your skills! If you’ve got experience with Microsoft Office, make sure to highlight that in conversations. Maybe even bring examples of how you’ve used it effectively in past roles. We want to see you demonstrate your expertise in a way that stands out!
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets seen. Plus, we’re always on the lookout for passionate candidates like you. Don’t miss out on the chance to join a global leader in clinical research – hit that apply button today!
We think you need these skills to ace Senior Clinical Research Associate: Single Sponsor (UK) in Livingston
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 skills align with the role, so don’t be shy about showcasing your on-site monitoring experience and any specific protocols you’ve worked with.
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 makes you a perfect fit for our team. We love seeing genuine enthusiasm!
Show Off Your Communication Skills: Since strong communication is key for this role, make sure your application reflects that. Whether it’s through clear language in your CV or a well-structured cover letter, we want to see how you convey your ideas effectively.
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’re considered for the role. Plus, it’s super easy to do!
How to prepare for a job interview at IQVIA LLC
✨Know Your Stuff
Make sure you brush up on your clinical research knowledge, especially around protocols and regulations. Familiarise yourself with the specific studies the company is involved in, as this will show your genuine interest and understanding of their work.
✨Showcase Your Experience
Be ready to discuss your previous on-site monitoring experience in detail. Prepare examples of how you've ensured compliance and managed study progress, as well as any challenges you've faced and how you overcame them.
✨Communication is Key
Since strong communication skills are a must, practice articulating your thoughts clearly and confidently. Think about how you can convey complex information simply, as this will be crucial when liaising with sites and stakeholders.
✨Get Tech-Savvy
Proficiency in Microsoft Office is required, so make sure you're comfortable using it. Consider preparing a few examples of how you've used these tools in your previous roles to enhance efficiency or improve documentation processes.
