Senior Clinical Research Coordinator – Oncology Trials

American Oncology Management Company; Houston (TX); On-site; USD 61,000 - 88,000; Full time

Job summary

Oncology Consultants is seeking a Senior Clinical Research Coordinator to coordinate the clinical trial process from site initiation through close-out at the Medical Center CCO Office in Houston. You will support the Principal Investigator and study team in screening, enrollment, informed consent, and patient care under GCP and FDA guidelines.

The role requires strong data management, regulatory submission experience, and the ability to train and mentor staff, with communication across

Qualifications

• Minimum 5 years of clinical research experience.
• Bachelor's or higher degree in health sciences.
• SOCRA or ACRP certification encouraged.

Responsibilities

• Coordinate study start-up, regulatory submissions, and initiation.
• Recruit and enroll patients and manage logs.
• Attend clinic visits and assist with study procedures.
• Maintain study documentation and data management.
• Communicate with investigators, sponsors, and staff.

Skills

Clinical research

Study coordination

Regulatory compliance

IRB submissions

Education

Degree in life sciences or health sciences

Job description

Oncology Consultants is seeking a Senior Clinical Research Coordinator to coordinate the clinical trial process from site initiation through close-out at the Medical Center CCO Office in Houston. You will support the Principal Investigator and study team in screening, enrollment, informed consent, and patient care under GCP and FDA guidelines.

The role requires strong data management, regulatory submission experience, and the ability to train and mentor staff, with communication across