Clinical Trials Associate – Europe – Remote

Job Overview

Worldwide Clinical Trials is seeking a Clinical Trials Associate for a remote role across Europe. You will contribute to the successful execution of clinical trials, supporting development-driven biopharmaceutical companies globally, ensuring adherence to regulatory standards and timely project completion.

Company Overview

Worldwide Clinical Trials (Worldwide) is a global CRO serving development-driven biopharmaceutical companies, with more than 4,400 professionals operating across more than 70 countries. The company delivers therapeutically dedicated expertise in neuroscience, oncology, rare disease, and internal medicine, with comprehensive support across every development phase – from early-stage and first-in-human studies through Phase III registration trials. The company’s flexible service model – spanning full-service trial management to functional service partnerships through Worldwide Flex – is powered by a people first, partnership driven outsourcing approach that strengthens collaboration, enhances data transparency, and supports more informed decision making. This provides sponsors with tailored, adaptable solutions that keep pace with the evolving demands of clinical research. Learn more at www.worldwide.com

Quick Details

• Salary Range: Market Competitive
• Job Type: Full-time
• Experience: 2 Year+
• Qualifications: None / Open to all applicants

Key Responsibilities

• Support the coordination and administrative aspects of assigned clinical trials.
• Assist in the preparation, review, and distribution of essential trial documents.
• Facilitate communication between investigative sites, sponsors, and internal teams.
• Track study progress, ensuring data accuracy and compliance with timelines.
• Maintain accurate and up-to-date trial master files (TMFs) or electronic trial master files (eTMFs).
• Ensure all trial activities adhere to Good Clinical Practice (GCP) and regulatory requirements.

Requirements

• Minimum of 2 years of experience in clinical research or a related healthcare field.
• Strong organizational skills and meticulous attention to detail.
• Excellent written and verbal communication skills for a remote, international setting.
• Ability to work independently and effectively manage multiple priorities.
• Proficiency with clinical trial management systems and Microsoft Office Suite.
• Understanding of clinical trial processes, regulatory requirements, and GCP guidelines.

Benefits

• Opportunity to work remotely from anywhere in Europe.
• Be part of a leading global Contract Research Organization (CRO).
• Engage in diverse and impactful clinical trials across various therapeutic areas.
• Competitive salary and comprehensive benefits package.
• Continuous professional development and career advancement opportunities.
• Collaborative and supportive work environment with a focus on innovation.