Join to apply for the Clinical Data Co-Ordinator role at Cancer Trials Ireland
This position involves performing Clinical Data Co-ordinator tasks on assigned studies within Cancer Trials Ireland, ensuring compliance with ICH-GCP, regulatory requirements, SOPs, and study protocols.
Key Requirements
* Third level degree in biomedical/life science or related discipline.
* Proficiency in Microsoft Office Tools and general computer literacy.
* Good organisational, communication, and time management skills.
* Attention to detail.
* Ability to work independently and as part of a team, meeting deadlines.
* Experience in Clinical Data Management or with EDC systems like iMedidata Rave is an advantage.
* Data analytics experience (e.g., Power BI, Python) is an advantage.
* An oncology background or relevant medical experience is an advantage.
Main Responsibilities
* Manage data tasks from study start-up to close-out, including database build and archiving.
* Support development and testing of CRFs, databases, and edit specifications.
* Review data for accuracy, completeness, and consistency.
* Ensure data quality and regulatory compliance.
* Participate in team meetings and collaborate with stakeholders.
* Maintain data management documentation and audit readiness.
* Provide administrative support to the Biometrics department as needed.
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