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 Clinical Data Risk Analyst at ICON, you will identify and mitigating risks associated with clinical trial data. You will contribute to the overall success of our clinical programs by employing risk assessment methodologies to ensure data integrity and compliance with regulatory standards.
What You Will Do
Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.
Key Responsibilities Include
Conducting risk assessments on clinical trial data to identify potential issues and recommend mitigation strategies.
Collaborating with global cross-functional teams to develop and implement risk management plans and protocols.
Monitoring data quality and integrity throughout the trial process,
reporting findings to stakeholders.
Utilizing statistical analysis and visualization tools to communicate risk-related insights effectively.
Supporting the preparation of risk management documentation for regulatory submissions and audits.
Your Profile
You will bring relevant clinical research experience, along with the following qualifications and skills.
Required Qualifications And Experience
Degree in life sciences or a related field.
3+ years clinical trials experience
Strong analytical and technical skills
Attention to detail and a proactive approach to identifying and addressing data risks.
Effective communication skills, with the ability to collaborate across diverse integral teams and convey complex information clearly.
What ICON Can Offer You
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 tale