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For Companies At a Glance
- Tasks: Support clinical study teams and manage essential trial documentation.
- Company: Join a life sciences company dedicated to innovative treatments for rare medical conditions.
- Benefits: Enjoy career growth, competitive salary, and a collaborative team environment.
- Why this job: Be part of cutting-edge research that makes a real impact on patients' lives.
- Qualifications: Experience in clinical trials and strong organisational skills are essential.
- Other info: On-site presence in West London is required 2 days a week.
The predicted salary is between 30000 - 42000 £ per year.
About Us
We are a specialised life sciences company focused on advancing innovative treatments for patients with rare and serious medical conditions. With a strong track record in clinical research and regulatory compliance, our team is dedicated to delivering meaningful impact where it's needed most.
About the Role:
We are seeking a detail-oriented and proactive Clinical Trial Assistant (CTA) to join our dynamic team within the Life Sciences industry. This role is ideal for someone who is passionate about clinical research and is looking to grow within a supportive and innovative environment. Please note: on-site presence in our West London office is mandatory 2 days per week.
Key Responsibilities:
- Provide administrative support to clinical study teams across multiple trials
- Maintain and update Trial Master Files (TMFs) in accordance with regulatory standards
- Assist with ethics submissions, investigator site files, and essential document tracking
- Support meeting preparation, minutes, and follow-ups
- Coordinate with CROs, vendors, and internal stakeholders
- Ensure adherence to GCP, SOPs, and company quality standards
Requirements:
- Proven experience working as a CTA or in a similar role within the Life Sciences sector
- Strong understanding of clinical trial processes and regulatory guidelines (ICH-GCP)
- Exceptional organizational and multitasking skills
- Excellent written and verbal communication
- Proficient in Microsoft Office Suite and clinical trial management systems (CTMS, eTMF)
- Ability and commitment to work from the West London office at least 2 days per week
What We Offer:
- Opportunity to work on cutting-edge clinical research projects
- Career progression and professional development support
- Collaborative and inclusive team environment
- Competitive salary and comprehensive benefits package
Ready to apply? If you meet the criteria and are excited to contribute to innovative life sciences research, we would love to hear from you!
Clinical Trial Associate (England) employer: EPM Scientific
Contact Detail:
EPM Scientific Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Associate (England)
✨Tip Number 1
Familiarise yourself with the latest trends and regulations in clinical trials, especially ICH-GCP guidelines. This knowledge will not only help you during interviews but also demonstrate your commitment to the field.
✨Tip Number 2
Network with professionals in the life sciences sector, particularly those who work as Clinical Trial Associates. Attend industry events or join relevant online forums to gain insights and potentially get referrals.
✨Tip Number 3
Prepare to discuss specific examples from your past experiences that showcase your organisational skills and ability to multitask. Highlighting these competencies can set you apart from other candidates.
✨Tip Number 4
Make sure to express your enthusiasm for working in a collaborative environment during your interactions with us. We value team players who are eager to contribute to innovative projects.
We think you need these skills to ace Clinical Trial Associate (England)
Some tips for your application 🫡
Understand the Role: Read the job description thoroughly to grasp the key responsibilities and requirements. Tailor your application to highlight your relevant experience as a Clinical Trial Associate or in a similar role.
Highlight Relevant Experience: In your CV and cover letter, emphasise your experience with clinical trial processes, regulatory guidelines, and any administrative support roles you've held. Use specific examples to demonstrate your skills.
Showcase Your Skills: Make sure to mention your organisational and multitasking abilities, as well as your proficiency in Microsoft Office Suite and clinical trial management systems. These are crucial for the role.
Craft a Compelling Cover Letter: Write a personalised cover letter that expresses your passion for clinical research and your desire to grow within the life sciences industry. Mention why you are excited about this opportunity and how you can contribute to the team.
How to prepare for a job interview at EPM Scientific
✨Know Your Clinical Trial Basics
Make sure you brush up on your knowledge of clinical trial processes and regulatory guidelines, especially ICH-GCP. Being able to discuss these topics confidently will show that you're well-prepared and understand the industry's standards.
✨Showcase Your Organisational Skills
As a Clinical Trial Associate, you'll need exceptional organisational skills. Prepare examples from your past experiences where you've successfully managed multiple tasks or projects simultaneously, highlighting your ability to stay organised under pressure.
✨Prepare for Team Collaboration Questions
Since the role involves coordinating with various stakeholders, be ready to discuss your experience working in teams. Think of specific instances where you contributed to a team project or resolved conflicts effectively.
✨Demonstrate Your Communication Skills
Excellent written and verbal communication is crucial for this role. Practice articulating your thoughts clearly and concisely, and consider preparing a few questions to ask the interviewers to demonstrate your engagement and interest in the role.
