Gynecologic Oncology Clinical Research Coordinator

Southwest-Women; Albuquerque (NM); On-site; USD 52,000 - 78,000; Full time

Benefits offered by this job

Health benefits

401(k)

Paid time off

Professional development

Job summary

Southwest Women's Oncology in Albuquerque, New Mexico seeks a Clinical Research Coordinator to manage day-to-day coordination of gynecologic oncology trials from start-up to close-out with independence and precision.

You will collaborate with investigators, sponsors, and the clinical team to ensure regulatory compliance, rigorous data integrity, and patient-centered trial care, contributing to enrollment and audit readiness.

Qualifications

• 2+ years of clinical research experience with trial coordination ownership.
• Working knowledge of GCP, ICH guidelines, and FDA regulatory requirements.
• Experience with electronic data capture (EDC) systems and regulatory file management.
• Strong knowledge of medical terminology and EMR systems.
• Exceptional organizational skills with attention to detail; able to manage multiple protocols.
• Compassionate, patient-centered approach in trial participation.

Responsibilities

• Coordinate Phase I–III gynecologic oncology trials from start-up through close-out.
• Lead regulatory submissions and site initiation logistics with IRBs and sponsors.
• Maintain study documents, regulatory files, and patient charts; ensure audit-readiness.
• Enter and manage study data in EDC systems; resolve data queries promptly.
• Support adverse event reporting and sponsor/CRO communications.

Skills

Clinical trial coordination

Regulatory compliance

Data management

GCP/ICh/FDA knowledge

EDC systems

Education

Bachelor's degree

Tools

EDC software

Job description

Southwest Women's Oncology in Albuquerque, New Mexico seeks a Clinical Research Coordinator to manage day-to-day coordination of gynecologic oncology trials from start-up to close-out with independence and precision.

You will collaborate with investigators, sponsors, and the clinical team to ensure regulatory compliance, rigorous data integrity, and patient-centered trial care, contributing to enrollment and audit readiness.