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- Tasks: Conduct site monitoring and manage clinical trial protocols for groundbreaking research.
- Company: Leading global clinical research firm with a strong reputation in the UK.
- Benefits: Career development opportunities in a dynamic and supportive environment.
- Why this job: Make a real difference in clinical trials while advancing your career.
- Qualifications: 18 months of independent monitoring experience and a life science degree.
- Other info: Join a team that values innovation and compliance in clinical research.
The predicted salary is between 36000 - 60000 £ per year.
A leading global clinical research firm in the UK is seeking an experienced Clinical Research Associate to conduct site monitoring and manage clinical trial protocols.
Responsibilities include:
- Performing monitoring visits
- Driving subject recruitment
- Ensuring compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Candidates should have at least 18 months of independent monitoring experience and a life science degree. This role offers career development opportunities in a dynamic environment.
Senior Clinical Research Associate - On-Site Monitoring Leader in Reading employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Research Associate - On-Site Monitoring Leader in Reading
✨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! Research the company and its recent projects, especially in clinical trials. Being knowledgeable about their work will show you're genuinely interested and ready to contribute.
✨Tip Number 3
Showcase your monitoring experience! Be ready to discuss specific examples of how you've driven subject recruitment and ensured compliance with GCP and ICH guidelines. Real-life stories make you memorable!
✨Tip Number 4
Don't forget to apply through our website! We’ve got loads of resources to help you land that Senior Clinical Research Associate role. Plus, it’s a great way to get noticed by our hiring team.
We think you need these skills to ace Senior Clinical Research Associate - On-Site Monitoring Leader in Reading
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in clinical research and monitoring. We want to see how your skills align with the responsibilities mentioned in the job description, so don’t hold back on showcasing your independent monitoring experience!
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, so let your personality come through!
Showcase Your Knowledge of GCP and ICH Guidelines: Since compliance is key in this role, make sure to mention your familiarity with Good Clinical Practice and International Conference on Harmonization guidelines. We’re looking for candidates who understand the importance of these standards in clinical trials.
Apply Through Our Website: We encourage you to apply directly through our website for a smoother application process. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates from our team!
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. Being able to discuss these in detail will show that you’re not just familiar with them, but that you truly understand their importance in clinical trials.
✨Showcase Your Monitoring Experience
Prepare specific examples from your past monitoring visits. Highlight challenges you faced, how you overcame them, and the impact of your actions on subject recruitment and compliance. This will demonstrate your hands-on experience and problem-solving skills.
✨Research the Company
Take some time to learn about the clinical research firm you’re interviewing with. Understand their values, recent projects, and any unique methodologies they employ. This knowledge will help you tailor your answers and show genuine interest in the role.
✨Ask Insightful Questions
Prepare thoughtful questions to ask at the end of your interview. Inquire about their approach to site monitoring or how they support career development for their staff. This not only shows your enthusiasm but also helps you gauge if the company is the right fit for you.
