Oncology Clinical Research Coordinator

American Oncology Network; Georgia; On-site; USD 44,000 - 74,000; Full time

Job summary

Oncology Consultants is seeking a Clinical Research Coordinator to join the research team involved in multiple facets of clinical trial management. The role supports start-up, regulatory submissions, site initiation, and patient recruitment under supervision by the Clinical Research Manager and Research Director.

Responsibilities include coordinating study visits, ensuring protocol compliance, collecting data, and maintaining documentation for sponsor monitoring and audits. Travel is possible.

Qualifications

• 2+ years of clinical research experience.
• Education in life sciences or health sciences as RN/PhD/MD or related degree.
• Certifications in SOCRA or ACRP are encouraged.

Responsibilities

• Support study start-up, regulatory submissions and site initiation to ensure protocol compliance.
• Assist IRB submissions and preparation for FDA inspections.
• Coordinate patient recruitment, screening and enrollment per protocol.
• Maintain study documentation, source data and queries for sponsor/audits.
• Provide administrative support and education to the research team.

Education

Life sciences/health sciences degree (RN, PhD, MD)

2+ years clinical research experience

Tools

SOCRA certification

ACRP certification

NIH training

IATA training

Job description

Oncology Consultants is seeking a Clinical Research Coordinator to join the research team involved in multiple facets of clinical trial management. The role supports start-up, regulatory submissions, site initiation, and patient recruitment under supervision by the Clinical Research Manager and Research Director.

Responsibilities include coordinating study visits, ensuring protocol compliance, collecting data, and maintaining documentation for sponsor monitoring and audits. Travel is possible.