Oncology Clinical Trial Lead

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

Job summary

Oncology Consultants is seeking a Senior Clinical Research Coordinator to oversee coordination of the clinical trial process from site initiation to close-out. You will support Principal Investigators, assist with informed consent, and manage data collection across multiple trials.

The role requires strong regulatory experience, patient recruitment skills, and collaboration with sponsors, IRBs, and study teams. AON-style competitive benefits are implied by the posting.

Qualifications

• 5+ years of clinical research experience.
• Certification in clinical research (SOCRA/ACRP) encouraged.
• NIH Human Subjects training required every 2 years.
• IATA training required every 2 years.

Responsibilities

• Coordinate study start-up, regulatory submissions, and IRB protocols.
• Manage patient recruitment, enrollment, and follow-up visits.
• Assist in clinical trial execution and patient care activities.
• Maintain accurate data and documentation for sponsor monitoring and audits.
• Support program coordination and cross-team communication.

Skills

Clinical Research

Regulatory Compliance

GCP/IRB

Study Coordination

Patient Recruitment

Data Management

Education

Bachelor's or higher in life sciences

RN/BSN

PhD/MD (optional)

Job description

Oncology Consultants is seeking a Senior Clinical Research Coordinator to oversee coordination of the clinical trial process from site initiation to close-out. You will support Principal Investigators, assist with informed consent, and manage data collection across multiple trials.

The role requires strong regulatory experience, patient recruitment skills, and collaboration with sponsors, IRBs, and study teams. AON-style competitive benefits are implied by the posting.