Clinical Research Coordinator

Job Title: Clinical Research Coordinator (CRC)

Location: Fully Remote – Germany

Employment Type: Full-time, Permanent

Language Requirement: Native or Fluent German

About the Company

Our client is a leading next-generation, full-service Contract Research Organization (CRO) transforming how clinical trials are delivered.

The company combines a world-class clinical operations team with advanced AI-powered software to run faster, more reliable clinical studies for life sciences organizations. By integrating innovative technology with deep clinical expertise, they manage the end-to-end delivery of clinical trials , including study design, patient recruitment, data capture, monitoring, and project management.

Having supported 40+ sponsors across the US, UK, and Europe , the organization has successfully delivered studies significantly faster than traditional CRO models , helping accelerate the development of new treatments and therapies.

The Role

We are seeking an experienced Clinical Research Coordinator (CRC) to join a growing clinical operations team. This position offers the opportunity to work fully remotely within Germany , supporting innovative clinical studies across multiple therapeutic areas.

The CRC will play a key role in the coordination and execution of clinical trials , ensuring studies are conducted in compliance with protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.

This role is ideal for a motivated CRC looking to join a modern, technology-driven CRO environment while contributing to high-impact clinical research.

Key Responsibilities

• Coordinate day-to-day activities related to clinical trial execution
• Support site management and investigator communication
• Assist with patient recruitment, screening, and retention activities
• Maintain accurate and complete study documentation and regulatory files
• Ensure compliance with study protocols, GCP, and applicable regulatory requirements
• Assist with data collection, query resolution, and clinical data entry
• Collaborate closely with clinical operations, monitoring teams, and sponsors
• Support study start-up, ongoing trial management, and close-out activities
• Ensure all trial-related documentation is accurate, up-to-date, and audit-ready

Requirements

• Minimum 2+ years of experience working as a Clinical Research Coordinator within clinical trials
• Native or fluent German (written and spoken) is required
• Strong understanding of ICH-GCP guidelines and clinical research processes
• Experience supporting clinical trial coordination at site level or within a CRO
• Excellent organizational and communication skills
• Ability to manage multiple tasks in a fast-paced, remote working environment
• Proficiency in clinical trial systems and electronic data capture (EDC) platforms is advantageous

What’s on Offer

• Fully remote position within Germany
• Opportunity to work with a fast-growing, technology-driven CRO
• Exposure to innovative clinical trial models and international studies
• Collaborative, mission-driven environment focused on accelerating medical innovation