Clinical Trial Operations Specialist

📋 Description

• Responsible for the planning, coordination, and execution of trial activities in accordance with ICH-GCP standards.

• Facilitates collaboration with external entities to carry out clinical trials.

• Oversees the preparation, finalization, and storage of documentation pertaining to clinical trials.

• Ensures the proper setup and ongoing maintenance of both internal and external systems and tools.

⛳️ Requirements

• Must possess a university degree and/or equivalent professional education, along with a minimum of 5 years of experience in clinical trials.

• Excellent communication abilities.

• Proficient in Windows and MS Office applications (Word, PowerPoint, Excel, Outlook).

• Fluency in both written and spoken English, as well as the local language.

🏝️ Benefits

• Flexible work arrangements.

• Opportunities for professional development.