Clinical Oncology Research Assistant — Trials & Data Integrity

Ironwood Women's Centers

Scottsdale (AZ)

Sur place

USD 42 000 - 60 000

Plein temps

Il y a 8 heures
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Avantages offerts par ce poste

Health insurance
Dental & Vision
401K

Résumé du poste

Ironwood Cancer & Research Centers in Scottsdale, AZ seeks a qualified and experienced Research Assistant to manage and conduct clinical trials, ensuring studies follow protocol guidelines and good clinical practices. You will assist with regulatory files, data entry, CRFs, study drug accountability, monitoring visits, and coordination with Research Nurses, while maintaining education and compliance.

A background in Pharmacy Technician preferred; Associate or Bachelor's degree favored; we offer

Qualifications

  • Experience with regulatory documentation and data entry.
  • Familiarity with clinical trial processes and GCP guidelines.
  • Current IATA, human subjects protection training or GCP training desirable.

Responsabilités

  • Maintain regulatory files, data entry, drug receipt/storage/transport.
  • Ensure quality and integrity of data.
  • Ensure compliance with department standards and federal regulations and ICH guidelines.
  • Pursue ongoing education through continuing education programs.
  • Assist with lab processing and shipping.
  • Complete CRFs and resolve data queries within timelines.
  • Ensure proper study drug accountability.
  • Assist Research Nurses with regulatory documents.
  • Participate in initiation, monitoring, closeout, and audit visits.
  • Assist with orientation and ongoing education of staff in the research department.

Connaissances

Detail oriented
Organized
Communication and team work
Regulatory knowledge
Leadership

Formation

Associate or Bachelor's Degree
GCP/IATA training desirable

Description du poste

Ironwood Cancer & Research Centers in Scottsdale, AZ seeks a qualified and experienced Research Assistant to manage and conduct clinical trials, ensuring studies follow protocol guidelines and good clinical practices. You will assist with regulatory files, data entry, CRFs, study drug accountability, monitoring visits, and coordination with Research Nurses, while maintaining education and compliance.

A background in Pharmacy Technician preferred; Associate or Bachelor's degree favored; we offer

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