ICON in Mexico City is seeking a Clinical Data Coordinator I to support and execute data review activities contributing to clinical data integrity. The ideal candidate will have 1-2 years of clinical data management experience, basic knowledge of the drug development process, and familiarity with Clinical Data Management Systems like Medidata RAVE or Veeva. This role offers benefits such as health insurance, retirement planning, and a work-life balance focus. Join a diverse team committed to shaping the future of clinical research.
#J-18808-Ljbffr