Job Description

Clinical Research Coordinator I (CRC I)

Location: Orlando, FL (onsite, Monday–Friday, 8:00 AM – 5:00 PM)

Role Summary:

Join our growing team as a Clinical Research Coordinator I, contributing to the execution of high-volume clinical trials in nephrology. This role focuses on patient visits, lab work, data management, and supporting site operations, with opportunities for professional growth in a fast-paced environment.

Key Responsibilities:

• Conduct patient visits, including scheduling, blood draws, and lab processing (2–3 patients/day; 4–5 hour visits).
• Manage patient eligibility, informed consent, and record-keeping.
• Perform data entry, query resolution, and CTMS updates.
• Communicate with monitors and assist during weekly monitoring visits.
• Ensure protocol and regulatory compliance, including IRB reporting and adverse event documentation.
• Maintain study supplies, investigational product inventory, and organized site operations.

Essential Qualifications:

• 3–5 years of CRC experience with high-volume trials (15–20 active, 5–6 pending startup).
• Proficient in blood draws and lab procedures.
• Knowledge of CTMS platforms.
• GCP certification.
• Strong organizational, communication, and data management skills.

Preferred Skills:

• Bilingual (English/Spanish) a plus.
• Experience with SAE/AE reporting.

Core Competencies:

• Empathy and excellent bedside manner.
• Ability to handle challenging patient interactions professionally.
• Enthusiasm and commitment to patient safety and ethical research practices.

Why Join Us:

• Fast-growing SMO with multiple growth opportunities.
• Collaborative, team-oriented environment.
• Focused onsite role—no travel required.

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