As a Clinical Data Coordinator I you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
**What you will be doing**:
- Receives relevant local laboratory information from investigative sites and transcribes this information into the EDC system or into a template to be imported into the EDC system
- Crosschecks the information provided with the protocol to certify that all required analytes are accounted for
- Works with the Clinical Data Managers (CDMs), Clinical Research Associates (CRAs) and investigative sites to clarify any source documentation issues and obtain any further updates which might be needed
- Regular attendance at Clinical Data Management group meetings and any departmental trainings
- Other duties, as assigned.
**You are**:
- Bachelor’s Degree or equivalent experience in clinical research or similar field
- At least 1 (one)



year of clinical or lab data review experience with experience reviewing lab/analyte data and/or lab source documentation
- Experience with Electronic Data Capture (EDC) system(s) preferred
- Oncology and/or Inflammatory therapeutic area experience preferred
**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 talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
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