Clinical Trials Associate

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

📋 Description

• Assist with the coordination 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 seamless trial execution.

• Contribute to monitoring and reporting on clinical trial metrics and milestones.

• Assist in the design and analysis of clinical trials, interpreting complex medical data, and support the advancement of innovative treatments and therapies.

⛳️ Requirements

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

• Previous experience or a strong interest in clinical research.

• Understanding of clinical trial processes, regulations, and guidelines.

• Exceptional organizational and communication abilities.

• Capability to work collaboratively in a fast-paced environment with meticulous attention to detail.

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

• Proficiency in both German and English languages.

• Employment with ICON is contingent upon possessing the legal right to work in the country where the position is located.

🏝️ 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.