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For Companies At a Glance
- Tasks: Conduct site evaluations and manage operations for innovative biotech products.
- Company: Global leading Biotech company with a focus on innovation.
- Benefits: Competitive salary, health benefits, and opportunities for career advancement.
- Why this job: Make a significant impact in the biotech field while ensuring compliance and quality.
- Qualifications: Detail-oriented with a passion for clinical research and compliance.
- Other info: Join a dynamic team dedicated to advancing healthcare solutions.
The predicted salary is between 30000 - 42000 £ per year.
A global leading Biotech company is seeking a Clinical Specialist / Junior Clinical Research Associate in Egham, UK. The role involves conducting site evaluations and managing operations for the SCENESSE® distribution, ensuring compliance with ICH-GCP guidelines.
Responsibilities include:
- Monitoring data collection
- Maintaining communications with clinical sites
- Preparing submissions for regulatory authorities
We are looking for a detail-oriented individual ready to make a significant impact in the biotech field.
Clinical Research Specialist I — Site Setup & Monitoring in Egham employer: EPM Scientific
Contact Detail:
EPM Scientific Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Specialist I — Site Setup & Monitoring in Egham
✨Tip Number 1
Network like a pro! Reach out to professionals in the biotech field on LinkedIn or at industry events. A friendly chat can lead to opportunities that aren’t even advertised yet.
✨Tip Number 2
Prepare for interviews by brushing up on ICH-GCP guidelines and the specifics of SCENESSE® distribution. Show us you know your stuff, and you'll stand out from the crowd!
✨Tip Number 3
Don’t just apply; follow up! A quick email after submitting your application shows enthusiasm and keeps you on their radar. We love seeing candidates who are proactive!
✨Tip Number 4
Use our website to apply directly! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re serious about joining our team.
We think you need these skills to ace Clinical Research Specialist I — Site Setup & Monitoring in Egham
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical research and site management. We want to see how your skills align with the responsibilities mentioned in the job description, so don’t hold back!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about the biotech field and how you can contribute to our team. Keep it concise but impactful – we love a good story!
Showcase Your Attention to Detail: Since the role requires a detail-oriented individual, make sure your application is free from typos and errors. We appreciate clarity and precision, so double-check everything before hitting send!
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!
How to prepare for a job interview at EPM Scientific
✨Know Your ICH-GCP Guidelines
Familiarise yourself with the International Council for Harmonisation - Good Clinical Practice (ICH-GCP) guidelines. Being able to discuss these in detail will show your understanding of compliance, which is crucial for the role.
✨Prepare for Site Evaluation Questions
Expect questions about site evaluations and how you would approach them. Think of examples from your past experiences or hypothetical scenarios where you can demonstrate your analytical skills and attention to detail.
✨Showcase Your Communication Skills
Since maintaining communication with clinical sites is key, be ready to discuss how you’ve effectively communicated in previous roles. Use specific examples that highlight your ability to build relationships and manage expectations.
✨Understand Regulatory Submissions
Brush up on the process of preparing submissions for regulatory authorities. Be prepared to explain how you would ensure accuracy and compliance in your submissions, as this will reflect your readiness to take on responsibilities in the role.
