Oncology Clinical Trials Lead Coordinator

American Oncology Network, Inc.; Houston (TX); On-site; USD 61,000 - 88,000; Full time

Job summary

Oncology Consultants - Medical Center CCO Office is seeking a Senior Clinical Research Coordinator to oversee trial startup through close-out, coordinating with investigators and sponsors to ensure protocol adherence.

The role requires 5+ years of clinical research experience, strong regulatory knowledge (IRB, FDA/ICH), and hands-on data management and patient coordination across multiple studies.

Qualifications

• Degree in life sciences or health sciences such as RN, BS, PhD, MD, or equivalent.
• Minimum 5+ years of clinical research experience.
• Research certifications (SOCRA/ACRP) encouraged; NIH human subjects training every 2 years; IATA training every 2 years.

Responsibilities

• Coordinate study startup, regulatory submissions, and IRB documentation to ensure protocol compliance.
• Manage patient recruitment, enrollment, screening logs, and follow-up visits per protocol.
• Oversee data collection, case report forms, source documents, and sponsor monitoring visits.

Job description

Oncology Consultants - Medical Center CCO Office is seeking a Senior Clinical Research Coordinator to oversee trial startup through close-out, coordinating with investigators and sponsors to ensure protocol adherence.

The role requires 5+ years of clinical research experience, strong regulatory knowledge (IRB, FDA/ICH), and hands-on data management and patient coordination across multiple studies.