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For Companies At a Glance
- Tasks: Support clinical study teams and manage essential trial documentation.
- Company: Join a leading life sciences company dedicated to innovative treatments for rare medical conditions.
- Benefits: Enjoy a supportive work environment with opportunities for growth and development.
- Why this job: Be part of impactful clinical research while working in a dynamic team atmosphere.
- Qualifications: Experience as a Clinical Trial Assistant or similar role is required.
- Other info: On-site presence in West London is needed 2 days a week.
The predicted salary is between 36000 - 60000 £ 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
Clinical Trial Associate employer: EPM Scientific
Contact Detail:
EPM Scientific Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Associate
✨Tip Number 1
Familiarise yourself with the specific clinical trial processes and regulations relevant to our industry. Understanding Good Clinical Practice (GCP) guidelines and how they apply to your role will give you a significant edge during interviews.
✨Tip Number 2
Network with professionals in the life sciences sector, especially those who work as Clinical Trial Associates. Attend industry events or join online forums to gain insights and potentially get referrals that could help you land the job.
✨Tip Number 3
Demonstrate your attention to detail and organisational skills during any interactions with us. Whether it's through emails or conversations, showcasing these traits can set you apart as a candidate who is well-suited for the role.
✨Tip Number 4
Research our company’s recent projects and achievements in clinical research. Being knowledgeable about our work will not only impress us but also help you articulate how you can contribute to our mission during discussions.
We think you need these skills to ace Clinical Trial Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical trials and life sciences. Emphasise any roles where you provided administrative support or maintained regulatory documents, as these are key responsibilities for the Clinical Trial Associate position.
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 demonstrate your attention to detail and proactive nature, which are essential for this position.
Highlight Relevant Skills: In your application, clearly outline skills that align with the job description, such as knowledge of GCP, SOPs, and experience with Trial Master Files. Use examples to illustrate how you've applied these skills in previous roles.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors or inconsistencies. A polished application reflects your attention to detail, which is crucial for a Clinical Trial Associate.
How to prepare for a job interview at EPM Scientific
✨Show Your Passion for Clinical Research
Make sure to express your enthusiasm for clinical research during the interview. Share specific examples of what drew you to this field and how you stay updated on industry trends. This will demonstrate your commitment and genuine interest in the role.
✨Familiarise Yourself with Regulatory Standards
Since the role involves maintaining Trial Master Files and ensuring compliance with regulatory standards, it's crucial to have a solid understanding of GCP and SOPs. Brush up on these guidelines before the interview and be prepared to discuss how you've applied them in previous roles.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills and ability to handle challenges in clinical trials. Prepare for scenario-based questions by thinking of past experiences where you successfully navigated obstacles or contributed to a team effort.
✨Highlight Your Organisational Skills
As a Clinical Trial Associate, you'll need to manage multiple tasks efficiently. Be ready to provide examples of how you've organised projects or maintained documentation in previous positions. This will showcase your attention to detail and ability to prioritise effectively.
