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Site Management and Compliance Coordinator
hace 1 semana
About ICON
At ICON, we're committed to fostering an inclusive environment that drives innovation and excellence in healthcare intelligence and clinical research. Our mission is to shape the future of clinical development.
Job Summary
We're seeking a skilled Clinical Research Associate II to join our team. As a CRA II, you'll work closely with a large-scale, fast-paced team to identify, select, initiate, and close out investigational sites for clinical studies in phases II – IV.
Key Responsibilities
- Study set-up and monitoring, report completion, and documentation management
- Protocol, consent document submission for ethics/IRB approval and regulatory submission preparation
- Study cost efficiency management
- Study documentation and feasibility study preparation and review
- Potential training and mentoring of fellow CRAs
Requirements
- Minimum 12 months' experience in phase I-III trial monitoring as a CRA
- Previous experience in medium-sized studies, including study start-up and close-out
- Knowledge of ICH-GCP guidelines and ability to evaluate medical data
- Ability to meet tight deadlines
- Valid driver's license and willingness to travel internationally/domestically (at least 60% of the time)
Total Reward Package
We offer a comprehensive total reward package, including competitive base pay, variable pay, recognition programs, and best-in-class employee benefits. Our supportive policies and wellbeing initiatives are designed to support you and your family throughout your career.
