Oncology Clinical Trials Research Administrator

ADP, Inc.; Maumee (OH); On-site; USD 65,000 - 90,000; Full time

Job summary

Precision Oncology Research is seeking an experienced Research Administrator (RA) to assist the Research Operations Administrator with administrative and regulatory processes for clinical trials from startup through closeout. The RA will handle IRB submissions, regulatory document preparation, ISF, and binder maintenance, while supporting the Sr.

Director in day-to-day operations and PI oversight documentation.

Qualifications

• Minimum 5 years of administrative experience in research.
• Knowledge of GCP.
• Strong team-oriented, results driven and collaborative style.
• Certification in Human Subjects Protection, Good Clinical Practices (must be obtained within 30 days of hire).
• Strong organizational and communication skills.

Responsibilities

• Assist with oversight of administrative and regulatory processes related to clinical trials from startup to closeout (IRB submissions, regulatory document prep and collection).
• Support ISF, Pharmacy and Lab Binder maintenance, and monitoring visit prep and execution.
• Support Sr. Director, Research Site Operations and ROA in day-to-day program operations and PI oversight documentation.
• Prepare and disseminate clinical trial documents and submissions to CROs/pharma sponsors.
• Maintain trial-specific files and spreadsheets and coordinate monitoring visits with sponsor reps.

Skills

Administrative experience

GCP knowledge

Team collaboration

Communication skills

Organizational skills

Education

Bachelor’s degree or equivalent experience

Job description

Precision Oncology Research is seeking an experienced Research Administrator (RA) to assist the Research Operations Administrator with administrative and regulatory processes for clinical trials from startup through closeout. The RA will handle IRB submissions, regulatory document preparation, ISF, and binder maintenance, while supporting the Sr.

Director in day-to-day operations and PI oversight documentation.