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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 30000 - 42000 £ 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 trends and regulations in clinical trials, especially ICH-GCP guidelines. This knowledge will not only boost your confidence during interviews but also demonstrate your commitment to the field.
✨Tip Number 2
Network with professionals in the clinical research industry through platforms like LinkedIn. Engaging with current Clinical Trial Associates or attending relevant webinars can provide insights and potentially lead to referrals.
✨Tip Number 3
Prepare for potential interview questions by practising how you would handle specific scenarios related to trial documentation and compliance. This will help you articulate your problem-solving skills effectively.
✨Tip Number 4
Showcase your organisational skills by discussing any relevant projects where you managed multiple tasks or deadlines. Highlighting these experiences can set you apart from other candidates.
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 ensuring compliance with regulatory standards.
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 support clinical operations. Mention specific skills that relate to the job, such as your organisational skills and 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 experiences that demonstrate your ability to manage priorities effectively and maintain attention to detail.
✨Communicate Clearly
Effective communication is key in this role. Practice articulating your thoughts clearly and concisely, especially when discussing how you would coordinate meetings or communicate with stakeholders.
✨Prepare Questions for Them
Interviews are a two-way street. Prepare insightful questions about the company's approach to clinical trials, their team dynamics, or how they ensure compliance. This shows your genuine interest in the position and the organisation.
