Summary from listing
The Clinical Project Support Specialist provides global operational, administrative, logistical, and compliance support for phase I–IV clinical trials. Responsibilities include maintaining study documentation and trackers, managing study systems and eTMF, supporting audits and inspections, coordinating meetings and investigator communications, handling CRO and vendor logistics, and contributing to study submissions and process improvements. The role reports to the CTS Team Lead in GBS Barcelona and requires a relevant bachelor’s degree or equivalent, at least one year of clinical research or development experience, Veeva experience, strong Microsoft Office and analytical skills, and fluency in English.
