Clinical Trial Coordinator - FSP Team - Madrid

shipping ofstudy files, faxing and photocopying documents, assembling study documents, and

arranging meetings, etc.).

• Maintain Trial Master File documentation within the appropriate TMF platform, participate in

TMF QC, as assigned, and track and /archive as applicable.

• Audit and CAPA tracking.

• Set up and maintain clinical investigator files and documentation.

• Liaise with vendors, as needed, for study conduct such as printing study materials and/or

external systems access for study team members.

• Coordinate and plan study supply shipments with vendors.

• Maintain and confirm shipment information such as courier tracking numbers and

date of shipping and delivery.

• Prepare/assemble/ship supplies to sites pre-SIV: Study File Notebooks, CRFs, other

study-specific ancillary supplies (i.e., diary cards, patient visit reminders).

• Generate reports as needed, for example CTMS site contact information list.

• Perform other administrative duties as assigned by Line Manager, Project Managers or Clinical

Trial Lead.

Qualifications(Minimum Required):

• Diploma – Associate degree or equivalent.

• In lieu of the above requirement, candidates with 1-2 or more years of relevant Clinical Research experience in pharmaceutical or CRO industries may be considered.

• Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

• Language Skills Required: Speaking: English and local language

Experience (Minimum Required):

• Minimum one (I) year administrative experience or equivalent training.

• Good oral and written communication skills.

• Good organizational and time management skills.

• Computer literacy (Microsoft Office Suite (Word, Excel, PowerPoint)

• Preferred:

• Aptitude for handling and proof-reading numerical data, some spreadsheetsoftware

competency

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