CRO, Clinical Monitoring Support Associate

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

📋 Description

• Assisting in the operations of clinical trials to guarantee the integrity, accuracy, and compliance of the clinical data gathered during studies.

• Working closely with clinical monitors, project managers, and other stakeholders to ensure efficient trial execution and adherence to regulatory requirements.

• Organizing and managing clinical trial documentation, tracking the progress of studies, and aiding in the resolution of data queries.

• Upholding high-quality data standards and contributing to the overall success of clinical research initiatives.

⛳️ Requirements

• A Bachelor’s degree in life sciences, health sciences, or a relevant field.

• A fundamental understanding of clinical research processes and Good Clinical Practice (GCP) guidelines.

• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) as well as clinical trial management systems.

• Strong organizational abilities with a keen attention to detail and the capability to manage multiple tasks concurrently.

• Exceptional written and verbal communication skills in English.

🏝️ Benefits

• Medical and dental coverage

• Matching 401(k)

• Paid time off