Oncology CRA: Sponsor-Focused Clinical Trials

IQVIA Argentina; Durham (NC); On-site; USD 90,000 - 198,000; Full time

Job summary

IQVIA is seeking a Clinical Research Associate to ensure study sites operate smoothly and in line with GCP and ICH guidelines, supporting oncology trials. You will monitor site activities, coordinate with investigators, and support trial execution across oncology studies.

Responsibilities include site visits, recruitment tracking, protocol training, TMF/ISF documentation, and mentoring of clinical staff, with collaboration across study teams.

Qualifications

• BS Degree in a scientific discipline or healthcare preferred.
• Minimum 1 year of on-site monitoring experience in oncology; 2 years preferred.
• Strong understanding of GCP and ICH guidelines, with expertise in oncology protocols.
• Proficiency in Microsoft Office, excellent communication, and strong organizational and problem-solving abilities.

Responsibilities

• Site visits: selection, initiation, monitoring, and close-out visits per GCP/ICH guidelines.
• Recruitment plans: collaborate with sites to develop and track recruitment plans.
• Training & Communication: provide protocol training and maintain regular site communication.
• Quality Assurance: evaluate site practices for protocol adherence and elevate issues.
• Study Progress: track regulatory submissions, recruitment, enrollment, and data management.
• Documentation: maintain TMF and ISF per regulatory requirements.
• Mentorship: mentor clinical staff through co-monitoring and training visits.
• Collaboration: work with study team members to support project execution.
• Financial Management: manage site finances and retrieve invoices per local requirements.

Education

BS Degree in a scientific discipline or healthcare

Job description

IQVIA is seeking a Clinical Research Associate to ensure study sites operate smoothly and in line with GCP and ICH guidelines, supporting oncology trials. You will monitor site activities, coordinate with investigators, and support trial execution across oncology studies.

Responsibilities include site visits, recruitment tracking, protocol training, TMF/ISF documentation, and mentoring of clinical staff, with collaboration across study teams.