A company is looking for a Clinical Research Associate focused on Oncology in Pennsylvania.
Key Responsibilities
Collaborate with teams to identify, select, and activate clinical trial sites
Perform Site Qualification Visits and ensure adherence to ICH-GCP guidelines and regulatory standards
Act as the main point of contact for sites and manage essential documents for site activation
Required Qualifications
B.S., R.N., or equivalent degree, preferably in Biological Sciences
2-3 years of experience in monitoring pharmaceutical industry clinical trials
1-3 years of experience monitoring oncology clinical trials
In-depth knowledge of Good Clinical Practice, ICH guidelines, and local regulatory requirements
Must be located in Pennsylvania, near a major airport
Pennsylvania Licensed Clinical Research Associate • Mesa, Arizona, United States