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- Tasks: Support clinical trials by managing documentation and coordinating communications.
- Company: Join a leading global CRO focused on innovative clinical research services.
- Benefits: Gain experience in a dynamic environment with opportunities for growth and learning.
- Why this job: Be part of impactful research that drives healthcare advancements globally.
- Qualifications: Bachelor’s degree in Life Sciences and 1-2 years in clinical research preferred.
- Other info: Ideal for those passionate about healthcare and eager to make a difference.
The predicted salary is between 28800 - 48000 £ per year.
Taylor Young is looking for a Clinical Trial Associate in the UK for a Global CRO. Join a leading global Contract Research Organization (CRO) dedicated to providing high-quality clinical research services to pharmaceutical, biotechnology, and medical device companies. With a global presence and a commitment to innovation, we drive efficiency and excellence across all phases of clinical development.
As a Clinical Trial Associate (CTA), you will support the clinical operations team in the planning, execution, and tracking of clinical trials across multiple therapeutic areas and global sites. You will be instrumental in maintaining trial documentation, coordinating project communications, and ensuring compliance with regulatory and company standards.
Key Responsibilities:
- Assist in the preparation, collection, and maintenance of essential clinical trial documents (eTMF/TMF).
- Support study start-up, conduct, and close-out activities in collaboration with Clinical Research Associates (CRAs), Project Managers (PMs), and regulatory teams.
- Track site submissions, approvals, and overall study timelines and milestones.
- Coordinate meetings, teleconferences, and documentation (e.g., agenda preparation, meeting minutes).
- Ensure compliance with ICH-GCP, SOPs, and applicable regulatory guidelines.
- Assist with budget tracking, vendor management, and investigator payments as needed.
- Support audit readiness by maintaining accurate and timely documentation.
- Communicate effectively with internal and external stakeholders including study sites, vendors, and sponsors.
Qualifications:
- Bachelor’s degree in Life Sciences, Healthcare, or a related field.
- 1–2 years of experience in a clinical research environment (ideally within a CRO).
- Strong understanding of clinical trial processes, ICH-GCP, and regulatory requirements.
- Proficiency in MS Office Suite (Word, Excel, Outlook) and clinical trial management systems (e.g., eTMF, CTMS).
- Excellent organizational skills with attention to detail and the ability to manage multiple priorities.
- Strong written and verbal communication skills.
- Ability to work independently and as part of a collaborative, cross-functional team.
Please apply if you are wanting more details!
Clinical Trial Associate employer: AL Solutions
Contact Detail:
AL Solutions Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Associate
✨Tip Number 1
Familiarise yourself with the latest trends and regulations in clinical trials. Understanding ICH-GCP guidelines and regulatory requirements will not only boost your confidence but also demonstrate your commitment to the role during interviews.
✨Tip Number 2
Network with professionals in the clinical research field. Attend industry events, webinars, or local meetups to connect with people who can provide insights about the role and potentially refer you to opportunities at StudySmarter.
✨Tip Number 3
Gain hands-on experience with clinical trial management systems (CTMS) and electronic trial master files (eTMF). If you haven't used these tools before, consider online courses or tutorials to enhance your skills, making you a more attractive candidate.
✨Tip Number 4
Prepare for potential interview questions by practising your responses to common scenarios faced by Clinical Trial Associates. Think about how you would handle challenges related to documentation, compliance, and communication, as these are key aspects of the role.
We think you need these skills to ace Clinical Trial Associate
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities of a Clinical Trial Associate. Familiarise yourself with the key tasks mentioned in the job description, such as maintaining trial documentation and supporting study activities.
Tailor Your CV: Customise your CV to highlight relevant experience in clinical research. Emphasise any previous roles that involved document management, compliance with regulatory standards, or collaboration with cross-functional teams.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your understanding of the role. Mention specific experiences that align with the job requirements, such as your familiarity with ICH-GCP guidelines or your proficiency in MS Office Suite.
Proofread Your Application: Before submitting, carefully proofread your application materials. Check for spelling and grammatical errors, and ensure that all information is clear and concise. A polished application reflects your attention to detail, which is crucial for this role.
How to prepare for a job interview at AL Solutions
✨Know Your Clinical Trial Basics
Make sure you have a solid understanding of clinical trial processes, ICH-GCP guidelines, and regulatory requirements. Brush up on your knowledge about essential documents like eTMF and TMF, as this will show your familiarity with the role.
✨Showcase Your Organisational Skills
As a Clinical Trial Associate, you'll need to juggle multiple tasks. Prepare examples from your past experience that demonstrate your ability to manage priorities effectively and maintain attention to detail, especially in documentation and compliance.
✨Communicate Clearly
Effective communication is key in this role. Practice articulating your thoughts clearly and concisely, both verbally and in writing. Be ready to discuss how you've successfully communicated with stakeholders in previous roles.
✨Prepare for Scenario Questions
Expect scenario-based questions that assess your problem-solving skills and ability to handle challenges in clinical trials. Think of specific situations where you had to coordinate with teams or manage timelines, and be prepared to explain your approach.
