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- Tasks: Manage clinical monitoring projects and ensure compliance with quality standards.
- Company: Join a growing team in the dynamic field of clinical research.
- Benefits: Competitive salary, potential for remote work, and opportunities for professional development.
- Why this job: Make a real impact in healthcare while working in a supportive and innovative environment.
- Qualifications: 2+ years in clinical trials and a relevant Life Science degree required.
- Other info: Applications close on 11th April, so apply soon!
The predicted salary is between 32000 - 36000 £ per year.
Location: UK-Based
Salary: £38,000 – £45,000
Start Date: May or June 2025
About the Role:
We are seeking an experienced Clinical Research Associate (CRA) I or II to join our clients growing team. In this role, you will be responsible for independently managing monitoring projects, ensuring timely delivery, and upholding the highest standards of quality and compliance.
Key Responsibilities:
- Independently manage assigned monitoring projects, keeping your Line Manager updated on progress against timelines and targets.
- Set up, manage, and maintain (e)TMFs in line with the (e)TMF Plan, SOPs, and project budgets.
- Ensure project milestones are met and invoiced as per contractual agreements.
- Deliver projects to a consistently high standard and format, obtaining additional input where required. Projects may include monitoring, regulatory submissions, and other activities as delegated.
- Maintain and manage study documentation and records, including filing within client eTMF systems, in compliance with SOPs.
- Liaise regularly with clients to discuss study progress and address any monitoring issues promptly.
- Ensure compliance with ICH-GCP and report any protocol or SOP breaches within agreed timelines.
- Develop training materials and deliver training in areas of expertise.
- Support process improvements across Clinical Operations activities.
- Assist Clinical Project Managers with start-up activities, regulatory and ethics submissions, system updates, and medical writing when required.
- Attend and coordinate meetings within budget guidelines.
- Perform additional tasks as requested on an ad hoc basis.
Requirements:
- Minimum 2 years of experience in clinical trials
- Bachelor’s degree (or higher) in a relevant Life Science discipline
- Full UK driving license and access to a car (preferred)
- Experience in independent monitoring (co-monitoring may be considered)
Important Information:
Due to high application volumes, this role will close for submissions on Friday 11th April.
Clinical Research Associate (South East) employer: Albion Rye Associates
Contact Detail:
Albion Rye Associates Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate (South East)
✨Tip Number 1
Network with professionals in the clinical research field. Attend industry conferences or local meetups to connect with CRAs and hiring managers. This can give you insights into the role and potentially lead to referrals.
✨Tip Number 2
Familiarise yourself with the latest regulations and guidelines in clinical research, particularly ICH-GCP. Being well-versed in these standards will demonstrate your commitment to quality and compliance during interviews.
✨Tip Number 3
Prepare to discuss specific projects you've managed in the past. Highlight your ability to meet deadlines and maintain high standards, as this is crucial for the role of a Clinical Research Associate.
✨Tip Number 4
Showcase your experience with eTMFs and project management tools. Being able to discuss your familiarity with these systems will set you apart, as they are essential for managing documentation and compliance.
We think you need these skills to ace Clinical Research Associate (South East)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical trials and monitoring projects. Use specific examples that demonstrate your ability to manage projects independently and ensure compliance with ICH-GCP.
Craft a Strong Cover Letter: Write a cover letter that addresses the key responsibilities outlined in the job description. Emphasise your experience in managing monitoring projects and your familiarity with (e)TMFs, as well as your commitment to quality and compliance.
Highlight Relevant Qualifications: In your application, clearly state your educational background, particularly your degree in a Life Science discipline. Mention any additional certifications or training that are relevant to the role of a Clinical Research Associate.
Follow Application Instructions: Ensure you submit your application before the deadline on Friday 11th April. Double-check that all required documents are included and formatted correctly, as this reflects your attention to detail.
How to prepare for a job interview at Albion Rye Associates
✨Know Your Clinical Trials
Make sure you brush up on your knowledge of clinical trials and the specific regulations that govern them. Being able to discuss ICH-GCP guidelines confidently will show your expertise and commitment to quality.
✨Demonstrate Project Management Skills
Prepare examples from your past experience where you've successfully managed monitoring projects. Highlight how you kept stakeholders updated and met project milestones, as this is crucial for the role.
✨Showcase Your Communication Skills
Since liaising with clients is a key responsibility, practice articulating how you've effectively communicated project progress and resolved issues in previous roles. Clear communication can set you apart.
✨Be Ready for Scenario Questions
Expect scenario-based questions that assess your problem-solving abilities. Think about potential challenges in clinical trials and how you would address them, demonstrating your proactive approach.
