Regulatory Technician

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ICON is a general healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

As a Regulatory Technician you will work with the Clinical Trials Information System (CTIS), and will also provide support for submissions and other documents by performing necessary tasks including assembly, dispatch among others and coordinating resources for submissions,

Responsibilities

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- Proactively identify and mitigate risks through CTIS helpdesks regarding data/document management and upload to CTIS and liaise with internal/external stakeholders to resolve




- Actively maintain applicable study-level account access for assigned projects for CTIS to maintain compliance and confidentiality
- Collaborate with key stakeholders to manage and perform data entry and document upload
- Monitor CTIS notifying applicable stakeholders of activities for their action and subsequent follow up
- Create files documenting submissions completed through CTIS, conclusions, decisions and any other communication provided via CTIS
- Perform Quality Control review in accordance with applicable process
- Maintain agreed timelines
- Ensure project-specific training is completed on time, as applicable

To succeed you will need

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- Mandatory advanced English (speak, read, write)
- Ideally you will have 1-2 years relevant experience within clinical research or have knowledge of clinical terminology and documentation
- Ability to work independently
- Experience with regulatory submissions and CTIS is a differential but not mandatory
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What ICON can offer you

📌 Regulatory Technician (Barcelona)
🏢 Icon Clinical Research
📍 Barcelona