Clinical Research Associate

Job Summary

To support innovative MedTech solutions, the part-time Clinical Research Associate will manage clinical trial activities, ensure compliance with regulatory standards, and collaborate with cross-functional teams in a remote setting.

Key responsibilities

• Manage and monitor clinical trial activities to ensure adherence to protocols and regulatory requirements
• Collaborate with internal teams and clients to facilitate project execution and communication
• Prepare and maintain study documentation and reports for regulatory submissions and audits

Required qualifications

• Bachelor's degree in a relevant field, such as life sciences or nursing
• Experience in clinical research or a related field
• Knowledge of Good Clinical Practice (GCP) and regulatory guidelines
• Proficiency in clinical trial management software and data management systems
• Ability to work independently and manage multiple projects simultaneously