Clinical Oncology Research Assistant — Trials & Data

Ironwood Cancer & Research Centers; Scottsdale (AZ); On-site; USD 48,000 - 60,000; Full time

Job summary

Ironwood Cancer & Research Centers in Scottsdale, AZ seeks a qualified Research Assistant - Clinical Oncology to support management and conduct of clinical trials in compliance with protocol guidelines and good clinical practices. The role is full-time and based at the Scottsdale office.

Key duties include regulatory file maintenance, data entry, data quality assurance, and assisting with study visits, drug accountability, and staff training.

Qualifications

• Experience with regulatory files and data entry is preferred.
• GCP or human subjects protection training is desirable.
• Knowledge of clinical trial processes and data integrity.

Responsibilities

• Assist with maintenance of regulatory files, data entry, drug receipt, storage, and transport.
• Ensure quality and integrity of data.
• Assist in ensuring compliance with department standards and regulatory guidelines (GCP).
• Support ongoing education and professional growth within the department.
• Assist with lab processing and study-related activities.
• Assist with CRFs and data entry/query resolution within protocol timelines.
• Assist with study drug accountability, including receipt, storage, dispensing, and transport.
• Support research nurses in maintaining regulatory documents.
• Participate in study initiation, monitoring, closeout, and audit visits.
• Assist with orientation and ongoing education of staff in the research department.

Skills

Excellent clinical skills

Organized and detail oriented

Strong leadership skills

Strong communication and teamwork

Education

Associate or Bachelor’s Degree preferred

Job description

Ironwood Cancer & Research Centers in Scottsdale, AZ seeks a qualified Research Assistant - Clinical Oncology to support management and conduct of clinical trials in compliance with protocol guidelines and good clinical practices. The role is full-time and based at the Scottsdale office.

Key duties include regulatory file maintenance, data entry, data quality assurance, and assisting with study visits, drug accountability, and staff training.