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- Tasks: Coordinate and manage clinical trials, ensuring patient safety and regulatory compliance.
- Company: Leading clinical research organisation focused on patient-centric studies.
- Benefits: Competitive salary and a supportive work environment.
- Why this job: Make a real difference in patient care through innovative clinical research.
- Qualifications: Bachelor's degree and 3 years of clinical trial experience required.
- Other info: Join a dynamic team dedicated to improving healthcare outcomes.
The predicted salary is between 36000 - 60000 £ per year.
A clinical research organization in the United Kingdom is seeking a Clinical Research Coordinator to manage Phase 2-4 clinical trials. Responsibilities include coordinating trial activities, ensuring patient safety, and maintaining compliance with regulatory standards.
The ideal candidate should have a Bachelor's degree in a relevant field and a minimum of 3 years of clinical trial experience. This role offers a competitive compensation package and is aimed at creating a more patient-centered clinical research environment.
Clinical Trials Coordinator — Patient-Centric Research in Bath employer: Civia Health
Contact Detail:
Civia Health Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trials Coordinator — Patient-Centric Research in Bath
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that Clinical Trials Coordinator role.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of patient-centric research. We recommend practising common interview questions and having examples ready that showcase your experience in managing clinical trials.
✨Tip Number 3
Don’t just apply anywhere; focus on organisations that align with your values. We suggest checking out our website for opportunities that resonate with your passion for patient safety and compliance in clinical trials.
✨Tip Number 4
Follow up after interviews! A simple thank-you email can set you apart from other candidates. We believe it shows your enthusiasm for the role and keeps you fresh in their minds.
We think you need these skills to ace Clinical Trials Coordinator — Patient-Centric Research in Bath
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in clinical trials. We want to see how your background aligns with the responsibilities of managing Phase 2-4 trials and ensuring patient safety.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about patient-centric research and how your skills can contribute to our mission. Keep it engaging and personal.
Showcase Your Compliance Knowledge: Since maintaining compliance with regulatory standards is key, be sure to mention any specific regulations or guidelines you’re familiar with. We love candidates who understand the importance of this aspect in clinical trials.
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 don’t miss out on any important updates from our team!
How to prepare for a job interview at Civia Health
✨Know Your Trials
Make sure you brush up on the specifics of Phase 2-4 clinical trials. Understand the processes involved, the importance of patient safety, and how compliance with regulatory standards plays a role in successful trial management.
✨Showcase Your Experience
Prepare to discuss your previous clinical trial experience in detail. Highlight specific projects you've managed, challenges you've faced, and how you ensured patient-centric approaches were at the forefront of your work.
✨Ask Insightful Questions
Come prepared with questions that show your interest in the organisation's approach to patient-centric research. Inquire about their strategies for enhancing patient engagement and how they measure success in their trials.
✨Demonstrate Compliance Knowledge
Familiarise yourself with the latest regulatory standards relevant to clinical trials in the UK. Be ready to discuss how you have maintained compliance in past roles and how you would ensure it in this position.
