Oncology CRA - Sponsor-Driven Impact

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

Job summary

IQVIA is seeking a Clinical Research Associate to ensure study sites run smoothly and in full compliance with GCP/ICH guidelines. You will conduct site visits, support patient recruitment, and train site staff to maintain high-quality data and regulatory documentation.

The role involves close collaboration with the study team, monitoring progress, and managing site finances. Oncology experience and strong communication skills are required to excel in this position.

Qualifications

• BS degree in a scientific discipline or healthcare preferred.
• Minimum 1 year of on-site monitoring experience in oncology; 2 years preferred.
• Strong knowledge of GCP and ICH guidelines, with oncology protocol expertise.
• Proficiency in Microsoft Office and excellent communication and organizational skills.
• Ability to manage time and financial aspects and build strong relationships with study sites.

Responsibilities

• Site Visits: Conduct selection, initiation, monitoring, and close-out visits per GCP/ICH.
• Recruitment Drive: 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 raise quality issues.
• Study Progress: Track regulatory submissions, recruitment, enrollment, and data management.
• Documentation: Maintain TMF and ISF per regulatory requirements.
• Mentorship: Guide clinical staff through co-monitoring and training visits.
• Collaboration: Work closely with study team members to support execution.
• Financial Management: Manage site finances and retrieve invoices per local requirements.

Skills

Microsoft Office

Communication

Organization

Problem-solving

Education

BS Degree in a scientific discipline or healthcare

Job description

IQVIA is seeking a Clinical Research Associate to ensure study sites run smoothly and in full compliance with GCP/ICH guidelines. You will conduct site visits, support patient recruitment, and train site staff to maintain high-quality data and regulatory documentation.

The role involves close collaboration with the study team, monitoring progress, and managing site finances. Oncology experience and strong communication skills are required to excel in this position.