About this role
Job title: CDC II
About the Role ICON is a world-leading healthcare intelligence and clinical research organization. As a CDC II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. This role focuses on delivering clinical data management work to a high standard, collaborating with data scientists, project teams, and stakeholders.
What You'll Do
- 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.
What We're Looking For
- Bachelor's degree in Life Sciences or Healthcare.
- Intermediate knowledge of clinical data management within the pharmaceutical or biotechnology industry.
- Familiarity with data management software and systems (e.g., Medidata, Oracle RDC, 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.
Nice to Have
- Knowledge of regulatory guidelines and standards (ICH-GCP) is a plus.
Compensation & Benefits
- Competitive salary.
- Various annual leave entitlements.
- Health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings.
- Global Employee Assistance Programme LifeWorks with 24-hour access to a global network.
- Flexible country-specific optional benefits (childcare vouchers, bike purchase schemes, gym discounts, travel passes, health assessments, etc.).