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- Tasks: Manage on-site monitoring and ensure compliance with clinical trial protocols.
- Company: Global leader in clinical research services with a commitment to innovation.
- Benefits: Competitive salary, travel opportunities, and professional development.
- Why this job: Make a real difference in healthcare by ensuring clinical trials run smoothly.
- Qualifications: Life science degree and experience in managing clinical trials.
- Other info: Dynamic role with travel to various clinical sites across the UK.
The predicted salary is between 36000 - 60000 £ per year.
A global provider of clinical research services is seeking an experienced Clinical Research Associate to manage on-site monitoring and ensure compliance with regulatory requirements. Ideal candidates will have a life science degree and experience managing multiple clinical trial protocols.
Responsibilities include:
- Monitoring visits
- Evaluating site practices
- Maintaining documentation standards
This full-time role is based in Reading, Berkshire, with travel required to various clinical sites.
Senior Clinical Research Associate - Field Monitoring (UK) employer: IQVIA LLC
Contact Detail:
IQVIA LLC Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Research Associate - Field Monitoring (UK)
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field and let them know you're on the lookout for opportunities. You never know who might have a lead or can put in a good word for you.
✨Tip Number 2
Prepare for those interviews by brushing up on your knowledge of regulatory requirements and clinical trial protocols. We recommend practising common interview questions with a friend or even in front of the mirror to boost your confidence.
✨Tip Number 3
Showcase your experience! When you get the chance to speak with potential employers, highlight your past monitoring visits and how you've ensured compliance. Use specific examples to demonstrate your skills and achievements.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search!
We think you need these skills to ace Senior Clinical Research Associate - Field Monitoring (UK)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in clinical trials and monitoring. We want to see how your background aligns with the role, so don’t be shy about showcasing your life science degree and relevant skills!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for the Senior Clinical Research Associate position. Share specific examples of your past experiences that relate to managing multiple clinical trial protocols.
Showcase Your Attention to Detail: As a Clinical Research Associate, attention to detail is key. In your application, highlight instances where you’ve ensured compliance with regulatory requirements or maintained high documentation standards. We love candidates who can demonstrate this skill!
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 – just follow the prompts and submit your materials!
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 regulatory requirements and trial protocols. 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
Prepare to discuss your previous roles in detail, particularly any experience you have with on-site monitoring and managing multiple trials. Use specific examples to illustrate how you've ensured compliance and maintained documentation standards in past positions.
✨Ask Smart Questions
Think of insightful questions to ask during the interview. This could be about their current projects, team dynamics, or how they handle challenges in clinical trials. It shows you're engaged and serious about the role.
✨Be Ready for Travel Talk
Since the role involves travel to various clinical sites, be prepared to discuss your flexibility and willingness to travel. Highlight any previous experiences where you successfully managed travel logistics while maintaining high standards in your work.
