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
- Competitive salary and benefits package
