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Clinical Trial Assistant (CTA)

Next Code Placement

UK | United Kingdom

Not Disclosed

1 - 5 Years

Full Time - Permanent

Views:7

Applicants:0

Posted on 7 Oct, 2026

In Office

Job Description | Responsibilities

  • Support clinical trial activities and study teams.
  • Maintain trial documents, files, and tracking systems.
  • Assist with site communication and study coordination.
  • Track study timelines, submissions, and required documentation.
  • Ensure records follow GCP and regulatory requirements.

Overview

  • Industry - CRO, Clinical Research Organization, HR / OD / L&D / Training / Counselling / Coaching Firms
  • Job Role - Clinical Trial Assistant (CTA)
  • Employment type - Full Time - Permanent
  • Work Mode - In Office

Qualifications

  • Any Graduate - Any Specialization
  • Any Post Graduate - Any Specialization
  • Any Doctorate - Any Specialization

Job Related Keywords

Clinical Trials GCP Trial Documentation Study Coordination TMF Regulatory Compliance Site Management Clinical Research

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