Site qualification, initiation, monitoring, and close-out visits
ICON Clinical Research is seeking a Clinical Research Associate with expertise in late-phase Oncology/Hematology to monitor clinical trials, ensuring protocol compliance and data integrity. The ideal candidate will have at least one year of experience as a CRA and a relevant scientific degree, with strong organizational and communication skills
Job Summary
As a CRA II at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
Matching Summary
Match Score: 85
ICON Clinical Research is seeking a Clinical Research Associate with expertise in late-phase Oncology/Hematology to monitor clinical trials, ensuring protocol compliance and data integrity. The ideal candidate will have at least one year of experience as a CRA and a relevant scientific degree, with strong organizational and communication skills.
Skills & Requirements
Must-have
Late phase Oncology/Hematology experience
Clinical trial monitoring activities
Site qualification, initiation, monitoring, and close-out visits
Protocol compliance, data integrity, and patient safety
Willingness to travel approximately 60%
Nice-to-have
Fostering an inclusive environment
Driving innovation and excellence
Advancement of innovative treatments and therapies
Key Requirements
Bachelor's degree in scientific or healthcare-related field
Minimum of 1 year of experience as a Clinical Research Associate
Experience with hematology/oncology as CRA
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines