A company is looking for a Clinical Research Associate focused on Start Up in Oncology.
Key Responsibilities
Collaborate with teams to identify, select, and activate clinical trial sites
Perform Site Qualification Visits and ensure adherence to ICH-GCP guidelines
Act as the main point of contact for sites and manage essential documentation 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 in monitoring oncology hematology therapeutic area clinical trials
Study Start Up experience as a CRA is required
In-depth knowledge of Good Clinical Practice and local regulatory requirements
Clinical Research Associate • Kansas City, Missouri, United States