Senior Clinical Research Coordinator - Oncology Trials

American Oncology Management Company; Houston (TX); On-site; USD 44,000 - 74,000; Full time

Job summary

Oncology Consultants - Memorial City is seeking a Clinical Research Coordinator to join the research team. You will support study start-up, regulatory submissions, site initiation, and ensure compliance with protocols and IRB requirements.

You will manage patient recruitment, screening, enrollment, and data collection, while coordinating visits and maintaining accurate study documentation. Strong communication with sponsors and investigators is essential.

Qualifications

• 2+ years of clinical research experience.
• Degree in life or health sciences (RN, PhD, MD, etc.).
• SOCRA or ACRP certification encouraged.
• NIH protection of Human subjects online course annually.
• IATA training every 2 years.

Responsibilities

• Assist start-up regulatory submissions and IRB filings.
• Coordinate patient recruitment, screening and enrollment activities.
• Coordinate study visits and ensure protocol compliance.
• Maintain study documentation and support sponsor monitoring and audits.
• Support data management and audit readiness.

Skills

Regulatory compliance

IRB coordination

Patient communication

Data accuracy

Education

Life/health sciences degree (RN, PhD, MD, etc.)

Tools

IRB portal

Study management software

Job description

Oncology Consultants - Memorial City is seeking a Clinical Research Coordinator to join the research team. You will support study start-up, regulatory submissions, site initiation, and ensure compliance with protocols and IRB requirements.

You will manage patient recruitment, screening, enrollment, and data collection, while coordinating visits and maintaining accurate study documentation. Strong communication with sponsors and investigators is essential.