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 Competitive salary and benefits package