Job Description

Key Responsibilities:

• Assist with the coordination and management of clinical trials in compliance with regulatory requirements and study protocols.
• Communicate effectively with study participants, physicians, and research team members.
• Schedule and conduct study visits, including data collection, sample handling, and documentation.
• Maintain accurate and organized study records, including electronic data entry.
• Support study start-up activities, such as preparing regulatory submissions and creating study binders.
• Ensure adherence to Good Clinical Practice (GCP) guidelines and institutional policies.
• Help identify and address issues or challenges during the study process.

Qualifications:

• High school diploma or equivalent; college degree preferred but not required.
• Strong organizational skills and attention to detail.
• Excellent verbal and written communication skills.
• Bilingual in Spanish and English

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