Clinical Trial Associate

This is a fully remote position, open to applicants in Czechia.

📋 Description

• Assist in the management and administration of clinical trials, ensuring adherence to protocols and regulatory standards.

• Organize and maintain clinical trial documentation, including study files, essential documents, and regulatory submissions.

• Aid in the preparation of study-related materials, such as informed consent forms and case report forms.

• Collaborate with cross-functional teams to enhance communication and ensure the seamless execution of trials.

• Contribute to the monitoring and reporting of clinical trial metrics and milestones.

⛳️ Requirements

• At least 1 year of experience as a Clinical Trial Assistant (CTA) or in a similar role.

• A Bachelor's degree in a scientific or healthcare-related discipline.

• Previous experience or a strong interest in clinical research.

• Familiarity with clinical trial processes, regulations, and guidelines.

• Proficiency in both Czech and English languages.

• Exceptional organizational and communication abilities.

• Capacity to work collaboratively in a dynamic environment with keen attention to detail.

• Willingness to travel as necessary (approximately 10%).

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellbeing programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life assurance and disability coverage.

• Employee assistance programs and wellbeing resources.

• Opportunities for learning and development through structured training and career pathways.