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- Tasks: Ensure regulatory compliance for clinical trials and conduct site visits.
- Company: Join a respected sponsor company in the UK, focused on clinical research.
- Benefits: Enjoy flexible part-time hours and competitive pay while gaining valuable experience.
- Other info: This is a freelance position with a 0.5 FTE commitment for 12 months.
- Why this job: Be part of a dynamic team making a real impact in healthcare.
- Qualifications: Bachelor's degree in a scientific field and proven experience as a Clinical Research Associate.
The predicted salary is between 36000 - 60000 £ per year.
I am seeking a professional and experienced Clinical Research Associate to join the team in the UK or a respected Sponsor company I am partnered with. This is a freelance, part-time position with a 0.5 FTE commitment for a 12-month duration. The successful candidate will be responsible for regulatory activities related to clinical trials.
Responsibilities
- Oversee regulatory compliance for clinical trials in accordance with local and international regulations
- Coordinate with regulatory authorities and ethics committees for approvals and submissions
- Ensure documentation and reporting are in line with regulatory requirements
- Conduct site visits to assess regulatory compliance and provide support and guidance to site staff
- Collaborate with cross-functional teams to ensure regulatory milestones are achieved
Qualifications
- Bachelor's degree in a scientific or healthcare discipline
- Proven experience as a Clinical Research Associate in regulatory activities
- In-depth knowledge of regulatory requirements for clinical trials in the UK
- Strong understanding of ICH-GCP guidelines and other relevant regulations
- Excellent communication and interpersonal skills
- Ability to work independently and manage time effectively
Day-to-Day
As a Clinical Research Associate, you will be responsible for ensuring regulatory compliance throughout the lifecycle of clinical trials. This will involve liaising with regulatory authorities, conducting site visits, and maintaining accurate documentation to support regulatory submissions.
Benefits
- Opportunity to work on a part-time basis with a flexible schedule
- Gain valuable experience in regulatory activities within clinical research
- Collaborate with a dynamic and supportive team
- Competitive compensation package
Clinical research associate uk employer: Barrington James Limited
Contact Detail:
Barrington James Limited Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical research associate uk
✨Tip Number 1
Network with professionals in the clinical research field. Attend industry conferences, webinars, or local meetups to connect with other Clinical Research Associates and learn about potential job openings.
✨Tip Number 2
Stay updated on the latest regulatory changes and guidelines in the UK. This knowledge will not only enhance your expertise but also demonstrate your commitment to the role during interviews.
✨Tip Number 3
Consider reaching out to current or former employees of the companies you’re interested in. They can provide insights into the company culture and the specific skills that are valued in a Clinical Research Associate.
✨Tip Number 4
Prepare for interviews by practising common questions related to regulatory compliance and clinical trials. Being able to articulate your experience and knowledge clearly will set you apart from other candidates.
We think you need these skills to ace Clinical research associate uk
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience as a Clinical Research Associate, particularly focusing on regulatory activities. Use specific examples that demonstrate your knowledge of ICH-GCP guidelines and compliance with UK regulations.
Craft a Strong Cover Letter: Write a cover letter that clearly outlines your motivation for applying to this position. Emphasise your experience in clinical trials and your ability to work independently while managing time effectively. Mention any specific achievements that relate to regulatory compliance.
Highlight Relevant Qualifications: In your application, ensure you mention your Bachelor’s degree in a scientific or healthcare discipline. If you have any additional certifications or training related to clinical research or regulatory affairs, be sure to include those as well.
Proofread Your Application: Before submitting your application, carefully proofread all documents for spelling and grammatical errors. A polished application reflects your attention to detail, which is crucial in the field of clinical research.
How to prepare for a job interview at Barrington James Limited
✨Know Your Regulations
Familiarise yourself with the local and international regulations related to clinical trials. Be prepared to discuss specific guidelines, such as ICH-GCP, and how they apply to your previous experiences.
✨Showcase Your Experience
Highlight your past roles as a Clinical Research Associate, focusing on your regulatory activities. Use specific examples to demonstrate your understanding of compliance and your ability to manage documentation effectively.
✨Prepare for Scenario Questions
Expect questions that assess your problem-solving skills in real-world scenarios. Think about challenges you've faced in previous roles and how you navigated them, especially during site visits or regulatory submissions.
✨Emphasise Communication Skills
Since the role involves liaising with various stakeholders, be ready to discuss how you communicate complex regulatory information clearly and effectively. Provide examples of successful collaborations with cross-functional teams.