ICON plc is a global leader in healthcare intelligence and clinical research, dedicated to advancing medical science through innovative clinical trials. With a commitment to excellence, diversity, and inclusion, ICON fosters a dynamic work environment where professionals contribute to life-changing therapies and treatments.
Join a team that values collaboration, innovation, and professional growth, and be part of shaping the future of clinical development.
Job Description
Key Responsibilities:
- Assist the Data Management Study Lead in maintaining eCRF, Data Validation Specifications, and Study Procedures.
- Manage clinical and third-party data reconciliation based on edit specifications and data review plans.
- Track and communicate study progress and task metrics to stakeholders.
- Address data-related queries and recommend solutions.
- Identify root causes of data issues and implement systematic resolutions.
Qualifications & Skills:
- Bachelor’s degree in Life Sciences, Healthcare, or related field.
- Intermediate experience in clinical data management (pharma/biotech industry preferred).
- Familiarity with data management software (Medidata, Oracle RDC, etc.).
- Strong attention to detail and ability to work in a fast-paced environment.
- Excellent communication and teamwork skills.
- Knowledge of ICH-GCP guidelines is a plus.
Why Join ICON plc?
ICON offers a competitive salary and comprehensive benefits, including:
✔ Generous annual leave
✔ Health insurance for you and your family
✔ Retirement planning options
✔ Employee Assistance Programme (TELUS Health) – 24/7 support
✔ Life assurance
✔ Flexible benefits (childcare vouchers, gym discounts, travel passes, etc.)
ICON is an equal opportunity employer, committed to diversity and inclusion. We encourage all qualified candidates to apply, even if they don’t meet every requirement.
How to Apply
