Opportunity Description
CRC Associate (Northamptonshire)
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
As a CRC Associate at ICON, you will support clinical research activities to ensure high-quality data, protocol adherence, and patient safety.
**What You Will Do:**
You will contribute to clinical coordination activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
+ Supporting the setup, coordination, and day-to-day conduct of clinical studies in accordance with protocols, ICH-GCP, and applicable regulations.
+ Assisting with patient screening, informed consent documentation, and enrolment activities under the supervision of site staff.
+ Ensuring accurate and timely completion of...
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
As a CRC Associate at ICON, you will support clinical research activities to ensure high-quality data, protocol adherence, and patient safety.
**What You Will Do:**
You will contribute to clinical coordination activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
+ Supporting the setup, coordination, and day-to-day conduct of clinical studies in accordance with protocols, ICH-GCP, and applicable regulations.
+ Assisting with patient screening, informed consent documentation, and enrolment activities under the supervision of site staff.
+ Ensuring accurate and timely completion of...
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