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- Tasks: Support clinical study teams and manage Trial Master Files for multiple trials.
- Company: Join a life sciences company dedicated to innovative treatments for rare medical conditions.
- Benefits: Enjoy career progression, competitive salary, and comprehensive benefits while working in a supportive environment.
- Why this job: Be part of cutting-edge research and make a meaningful impact in healthcare.
- Qualifications: Detail-oriented with knowledge of clinical trial processes and proficiency in Microsoft Office.
- Other info: On-site presence in West London is required 2 days per week.
The predicted salary is between 36000 - 60000 £ per year.
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.
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.
- Provide administrative support to clinical study teams across multiple trials
- Maintain and update Trial Master Files (TMFs) in accordance with regulatory standards
- Ensure adherence to GCP, SOPs, and company quality standards
- Strong understanding of clinical trial processes and regulatory guidelines (ICH-GCP)
- 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
Opportunity to work on cutting-edge clinical research projects. Career progression and professional development support. Competitive salary and comprehensive benefits package.
Clinical Trial Associate/clinical Study employer: EPM Scientific
Contact Detail:
EPM Scientific Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Associate/clinical Study
✨Tip Number 1
Familiarise yourself with the latest developments in clinical trial processes and regulatory guidelines, especially ICH-GCP. This knowledge will not only help you stand out during discussions but also demonstrate your commitment to the field.
✨Tip Number 2
Network with professionals in the life sciences industry, particularly those involved in clinical research. Attend relevant conferences or webinars to make connections that could lead to valuable insights and potential referrals for the role.
✨Tip Number 3
Showcase your proficiency in Microsoft Office Suite and any clinical trial management systems you’ve used. If you have experience with eTMF, highlight this in conversations, as it’s a key requirement for the position.
✨Tip Number 4
Be prepared to discuss your organisational skills and attention to detail during interviews. Provide examples of how you've successfully managed multiple tasks or projects, as these are crucial traits for a Clinical Trial Associate.
We think you need these skills to ace Clinical Trial Associate/clinical Study
Some tips for your application 🫡
Understand the Role: Read the job description carefully to understand the responsibilities and requirements of the Clinical Trial Associate position. Highlight your relevant experience in clinical research and regulatory compliance.
Tailor Your CV: Customise your CV to reflect your skills and experiences that align with the role. Emphasise your proficiency in Microsoft Office Suite, CTMS, and eTMF, as well as your understanding of GCP and ICH-GCP guidelines.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your proactive approach. Mention specific examples of how you've contributed to clinical trials or maintained regulatory standards in previous roles.
Proofread Your Application: Before submitting, thoroughly proofread your application materials. Check for any spelling or grammatical errors, and ensure that all information is accurate and clearly presented.
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 any relevant experiences or projects that highlight your commitment to advancing innovative treatments, as this aligns with the company's mission.
✨Demonstrate Attention to Detail
As a Clinical Trial Associate, attention to detail is crucial. Be prepared to discuss how you ensure accuracy in your work, particularly when maintaining Trial Master Files and adhering to regulatory standards.
✨Familiarise Yourself with Regulatory Guidelines
Brush up on ICH-GCP and other regulatory guidelines before the interview. Being able to discuss these topics confidently will show that you understand the importance of compliance in clinical trials.
✨Highlight Your Technical Skills
Since proficiency in Microsoft Office Suite and clinical trial management systems is essential, be ready to provide examples of how you've used these tools in previous roles. This will demonstrate your capability to handle the administrative aspects of the job effectively.
