Trial Documentation Specialist (m/f)

REFERENZNUMMER:

349887/11

IHRE AUFGABEN:

-Track and review TMF/eTMF documents for completeness, accuracy, and quality within required timelines while maintaining consistency and attention to details
-Ensure documents are coded, indexed, scanned, and imported into the TMF/eTMF once the quality review is completed
-Create, track, and resolve document quality issues and/or missing documents in Clinical Trial Management System (CTMS)
-Ensure that the documents are uploaded into the eTMF system and are quality checked (e.g., all pages included, documents are legible, correct naming convention)

IHRE QUALIFIKATIONEN:

-High school diploma
-Administrative and clerical experience, preferably in a pharmaceutical setting
-Previous experience in electronic filing systems
-Strong computer skills, including working with the Microsoft suite of programs
-Demonstrated oral and written communication skills
-Fluency in English; fluency in other languages is advantageous

WEITERE QUALIFIKATIONEN:

Clinical trial assistant