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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: Enjoy a dynamic work environment with opportunities for growth and learning.
- Why this job: Be part of impactful research that drives healthcare advancements globally.
- Qualifications: Bachelor’s in Life Sciences; 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 - 43200 £ 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.
- 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 ICH-GCP guidelines and regulatory requirements. This knowledge will not only help you in interviews but also demonstrate your commitment to compliance, which is crucial for a Clinical Trial Associate role.
✨Tip Number 2
Network with professionals in the clinical research field, especially those working in CROs. Attend industry events or join relevant online forums to connect with potential colleagues and learn about the latest trends and opportunities.
✨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 taking online courses or tutorials to boost your proficiency.
✨Tip Number 4
Prepare to discuss specific examples of how you've managed multiple priorities in past roles. Being able to articulate your organisational skills and attention to detail will set you apart during the interview process.
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 or projects that align with the responsibilities of the CTA position, particularly your understanding of ICH-GCP and regulatory requirements.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your ability to contribute to the team. Mention specific experiences that demonstrate your organisational skills and attention to detail, which are crucial for this role.
Proofread Your Application: Before submitting, carefully proofread your application materials. Check for any spelling or grammatical errors, and ensure that all information is clear and concise. A polished application reflects your professionalism and attention to detail.
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 eTMF and CTMS systems, as these will likely come up during the interview.
✨Showcase Your Organisational Skills
As a Clinical Trial Associate, you'll need to juggle multiple tasks. Be prepared to discuss how you've managed competing priorities in the past, and provide examples of how your organisational skills have contributed to successful project outcomes.
✨Communicate Effectively
Strong communication skills are crucial for this role. Practice articulating your thoughts clearly and concisely, and be ready to demonstrate how you've effectively communicated with various stakeholders in previous roles.
✨Prepare Questions for Them
Interviews are a two-way street. Prepare thoughtful questions about the company's culture, team dynamics, and specific projects they are working on. This shows your genuine interest in the role and helps you assess if it's the right fit for you.
