Clinical Research Associate

Job Summary

Motivated and experienced professionals will find a full-time remote opportunity as a Clinical Research Associate, responsible for managing site interactions, overseeing clinical trial activities, and ensuring compliance with regulations while actively contributing to the success of global clinical studies.

Key responsibilities

• Manage and maintain continuous communication with clinical trial sites for the implementation of global clinical trials
• Conduct site management and monitoring activities, including on-site and remote visits, training of site staff, and independent management of centers
• Prepare and update study-related documents and ensure compliance with internal and external guidelines, ICH-GCP regulations, and SOPs

Required qualifications

• Degree in natural or health sciences or equivalent relevant education
• Experience in the clinical trials field
• Strong organizational skills and an outgoing personality with the ability to motivate others
• High degree of flexibility, teamwork, and strong communication skills
• Proficient in MS Office and fluent in English and German