ICON seeks a Regulatory Technician to support clinical trial submissions and data management through the Clinical Trials Information System (CTIS). The role involves document assembly, risk mitigation, stakeholder coordination, and quality control oversight across clinical research projects based in Barcelona or Madrid.

Responsibilities

- Identify and mitigate risks related to CTIS data and document management via helpdesks
- Maintain study-level account access and compliance for assigned projects
- Collaborate with stakeholders on data entry and document uploads to CTIS
- Monitor CTIS activities and notify stakeholders of actions requiring follow-up
- Perform quality control reviews and maintain submission timelines and project training schedules

Requirements

- Advanced English proficiency (speaking, reading, writing)
- 1-2 years clinical research experience or clinical terminology knowledge
- Ability to work independently and manage multiple tasks
- CTIS experience preferred but not required
- Regulatory submissions experience advantageous

📌 Regulatory Technician (España)
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📍 España