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 CDC (all levels) at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of creative treatments and therapies.
What You Will Do
Your role will involve delivering clinical data management work to a high standard, working closely with your team and stakeholders.
Key Responsibilities Include
Assist Data Management Study Lead in maintenance of eCRF, Data Validation Specifications, and Study Specific Procedures.
Manage clinical and third-party data reconciliation based on edit specifications and data review plans.
Tracks and communicates status of study and task metrics to clinical data scientist, project team, and functional management.
Address data related questions and recommend potential solutions.
Identify root cause to systematically resolve data issues.
Opportunity to support multiple programs and it is a client facing role.
Your Profile
You will bring relevant clinical data management experience, along with the following qualifications and skills.
Required Qualifications And Experience
Bachelor's degree in a relevant field, such as Life Sciences or Healthcare.
Minimum 1 - 5 years of experience in core CDM.
Familiarity with data management software and systems (e.g., Medidata Rave, Veeva EDC, Oracle Clinical, Red Cap RCC, or similar).
Strong attention to detail and the ability to work effectively in a fast-paced environment.
Excellent communication skills and the ability to collaborate with cross-functional teams.
Knowledge of regulatory guidelines and standards (e.g., ICH-GCP) is a plus.
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 cul