Phase I Oncology Research Specialist - Trial Start-Up

Advocate Health; Charlotte (NC); On-site; USD 42,000 - 62,000; Full time

Job summary

Advocate Health is seeking a detail-oriented professional to support oncology research projects and clinical trials. The role focuses on document control, study start-up activities, and ensuring regulatory compliance across protocols and informed consent processes.

You will maintain study documentation, assist in data systems, and help coordinate scheduling and patient eligibility checks within an audit-ready environment.

Qualifications

• High School Diploma or GED required; bachelor's degree preferred (Health/Science preferred).

Responsibilities

• Assists with documentation for oncology research projects/clinical trials.
• Participates in study start-up activities with the PI and team.
• Maintains protocol amendments, deviations, and informed consent changes.
• Maintains documentation for assigned studies.
• Assists in filing systems, data repositories and systems.
• Monitors clinical trial compliance and reports issues.
• Obtains and assesses patient eligibility for studies.
• Coordinates scheduling of tests and treatments with local staff.
• Collects data for patients enrolled on trials.

Education

High School Diploma or GED

Job description

Advocate Health is seeking a detail-oriented professional to support oncology research projects and clinical trials. The role focuses on document control, study start-up activities, and ensuring regulatory compliance across protocols and informed consent processes.

You will maintain study documentation, assist in data systems, and help coordinate scheduling and patient eligibility checks within an audit-ready environment.