Senior Clinical Research Coordinator (RN) – Oncology Trials

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

Job summary

Oncology Consultants in Houston, TX seeks an experienced Clinical Research Coordinator III (RN) to join our research team. The role supports study start-up, regulatory submissions, patient recruitment, and data management under the supervision of the Research Director.

Responsibilities include coordinating study visits, dispensing study drugs per protocol, consenting patients, and maintaining accurate source documents for sponsor monitoring and audits.

Qualifications

• RN or life sciences degree required; advanced degrees encouraged.
• Minimum 2 years of clinical research experience.
• SOCRA or ACRP certification encouraged; NIH human subjects course annually.
• IATA training required every 2 years.

Responsibilities

• Support study start-up, regulatory submissions and site initiation.
• Recruit, screen and enroll patients per protocol.
• Coordinate visits, dispense study drugs and manage samples.
• Maintain study documentation and assist with sponsor monitoring and audits.
• Support department operations, budgeting and training activities.

Skills

Clinical research

Regulatory submissions

Data management

Patient recruitment

IRB coordination

Study coordination

Education

RN

PhD

MD

Job description

Oncology Consultants in Houston, TX seeks an experienced Clinical Research Coordinator III (RN) to join our research team. The role supports study start-up, regulatory submissions, patient recruitment, and data management under the supervision of the Research Director.

Responsibilities include coordinating study visits, dispensing study drugs per protocol, consenting patients, and maintaining accurate source documents for sponsor monitoring and audits.