China - CTA
What you will be doing

• Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.

• Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.

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

• Work with cross-functional teams to facilitate communication and ensure smooth trial execution.

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

Your profile

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

• Prior experience or strong interest in clinical research.

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

• Excellent organizational and communication skills.

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