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 Competitive salary and benefits package