Clinical Trial Associate

EPM Scientific; London; On-site; GBP 30,000 - 40,000; Full time

Job summary

A leading life sciences company is seeking a detail-oriented Clinical Trial Assistant to support clinical study teams. The role involves maintaining regulatory compliance, assisting with submissions, and ensuring quality standards. Ideal for candidates passionate about clinical research and seeking career development in a collaborative environment.

Benefits

Career progression support

Collaborative team environment

Competitive salary and benefits

Opportunity on innovative projects

Qualifications

• Proven experience working as a CTA or in a similar role.
• Strong understanding of clinical trial processes.
• Able to work from the West London office at least 2 days a week.

Responsibilities

• Provide administrative support to clinical study teams.
• Maintain and update Trial Master Files (TMFs).
• Assist with ethics submissions and document tracking.

Skills

Organizational skills

Multitasking

Communication

Tools

Microsoft Office Suite

Clinical trial management systems

Job description

EPM Scientific are partnered with a specialised life sciences company who focus on advancing innovative treatments for patients with rare and serious medical conditions. With a strong track record in clinical research and regulatory compliance, their team is dedicated to delivering meaningful impact where it's needed most.

They are seeking a detail-oriented and proactive Clinical Trial Assistant (CTA) to join their 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.

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's on 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!