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- Tasks: Manage clinical trials and ensure compliance with ICH GCP guidelines.
- Company: Leading clinical research organisation in the UK with a focus on diversity.
- Benefits: Flexible working options and strong support for team members.
- Why this job: Make a real difference in participant welfare and clinical research.
- Qualifications: Degree in life sciences and 2-3 years of CRA experience.
- Other info: Join a diverse team committed to inclusivity and professional growth.
The predicted salary is between 36000 - 60000 £ per year.
A leading clinical research organization in the UK is seeking a Clinical Research Associate (CRA) to manage clinical trials and ensure compliance with ICH GCP guidelines.
Responsibilities include:
- Building relationships with study personnel
- Monitoring investigational sites
- Ensuring participant welfare is prioritized
The ideal candidate should have a degree in life sciences and 2-3 years of CRA experience. Opportunities for flexible working and support for team members are offered in a commitment to diversity and inclusivity.
CRA: Site Monitoring & Trial Data Integrity in London employer: Novotech
Contact Detail:
Novotech Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land CRA: Site Monitoring & Trial Data Integrity in London
✨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 CRA roles. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on ICH GCP guidelines and trial monitoring processes. 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 relationship-building skills! During interviews, share specific examples of how you've successfully collaborated with study personnel in the past. This will demonstrate your ability to thrive in a team-oriented environment.
✨Tip Number 4
Don't forget to apply through our website! We’ve got loads of opportunities that might be perfect for you. Plus, it’s a great way to ensure your application gets seen by the right people.
We think you need these skills to ace CRA: Site Monitoring & Trial Data Integrity in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in clinical trials and compliance with ICH GCP guidelines. We want to see how your background aligns with the role, so don’t be shy about showcasing your skills!
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 experience makes you the perfect fit for our team. Keep it engaging and personal – we love to see your personality!
Showcase Your Relationship-Building Skills: As a CRA, building relationships is key. In your application, mention specific examples of how you've successfully collaborated with study personnel or ensured participant welfare. We want to know how you connect with others!
Apply Through Our Website: We encourage you to apply directly through our website for a smoother 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 Novotech
✨Know Your ICH GCP Guidelines
Make sure you brush up on the ICH GCP guidelines before your interview. Being able to discuss these in detail will show that you understand the importance of compliance in clinical trials and that you're ready to ensure participant welfare.
✨Showcase Your Relationship-Building Skills
Since building relationships with study personnel is key, prepare examples from your past experiences where you've successfully collaborated with others. This will demonstrate your interpersonal skills and how you can contribute to a positive team environment.
✨Highlight Your Monitoring Experience
Be ready to talk about your previous site monitoring experiences. Discuss specific challenges you faced and how you overcame them, as this will illustrate your problem-solving abilities and your commitment to maintaining trial integrity.
✨Emphasise Flexibility and Inclusivity
With opportunities for flexible working and a focus on diversity, express your enthusiasm for these values. Share any relevant experiences that highlight your adaptability and commitment to inclusivity, showing that you align with the company's culture.
