Oncology Clinical Research Coordinator II - Trial Onboarding

Lumi Research; Houston (TX); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Two weeks PTO per year

Medical benefits monthly stipend

Job summary

Lumi Research is seeking an Oncology Clinical Research Coordinator II to oversee regulatory and patient consenting for clinical trials, ensuring data accuracy and compliant documentation. This role involves training new team members, coordinating study visits, and maintaining regulatory shares across protocols.

The coordinator will manage screening, consent, data entry, and adverse event reporting while supporting onboarding of patients and collaboration with clinician partners in a community

Qualifications

• Minimum 2–3 years of oncology clinical trial experience.
• Ability to obtain informed consent and register patients.
• Experience with regulatory documentation and trial monitoring.

Responsibilities

• Coordinate and attend study initiation visits and planning.
• Maintain protocol versions and consent forms per protocol.
• Prepare regulatory reports for trial monitoring and audits.
• Collect, document and maintain knowledge of adverse events.
• Assist with protocol annual reviews and toxicity reports as applicable.
• Maintain delegation and training logs and trial documentation.

Skills

Oncology knowledge

Independent worker

Critical thinking

Communication

Organization

Multitasking

Job description

Lumi Research is seeking an Oncology Clinical Research Coordinator II to oversee regulatory and patient consenting for clinical trials, ensuring data accuracy and compliant documentation. This role involves training new team members, coordinating study visits, and maintaining regulatory shares across protocols.

The coordinator will manage screening, consent, data entry, and adverse event reporting while supporting onboarding of patients and collaboration with clinician partners in a community