Position Overview:

We are seeking a motivated and detail-oriented individual to join our team as a Clinical Research Coordinator. This is an excellent opportunity for someone looking to build a career in clinical research. No prior experience is required, but we are looking for candidates with a proven track record of longevity in their previous roles, demonstrating commitment and reliability.

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.