Clinical Trial Associate

JR United Kingdom; Greater London; On-site; GBP 30,000 - 40,000; Full time

Job summary

A leading global Contract Research Organization is seeking a Clinical Trial Associate to support clinical operations in the UK. This role involves maintaining trial documentation, coordinating communications, and ensuring compliance with regulatory standards. Ideal candidates will have a background in Life Sciences and experience in clinical research, with strong organizational and communication skills.

Qualifications

• 1–2 years of experience in a clinical research environment.
• Strong understanding of clinical trial processes and regulatory requirements.

Responsibilities

• Assist in the preparation and maintenance of clinical trial documents.
• Support study start-up, conduct, and close-out activities.
• Ensure compliance with ICH-GCP and regulatory guidelines.

Skills

Organizational Skills

Communication

Attention to Detail

Education

Bachelor’s degree in Life Sciences

Bachelor’s degree in Healthcare

Tools

MS Office Suite

Clinical Trial Management Systems

Job description

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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.

Qualifications:

• 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!