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Trial Documentation Specialist (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Gesuchte Skills: Support
Projektbeschreibung
REFERENZNUMMER:
294157/11
IHRE AUFGABEN:
-Reviewing and processing of all documents received for the TMF with focus on reviewing, indexing, tracking, scanning and filing for IMP approved documents
-Ensure accurate set-up, maintenance and archiving of the TMF/eTMF within the required timeline
-Reading and QS reviewing of documents
-Support the trial management teams in the preparation, conduct, and follow up of internal and/or external audits/inspections
-Return the transmittal and confirmation of receipt (COR) of all required documents and send the COR back to the sender within the required timelines
IHRE QUALIFIKATIONEN:
-Profound administrative and clerical experience, preferably in a pharmaceutical setting
-Prior experience in working with electronic filing systems
-Strong computer skills including working Microsoft Suite
-Fluency in English
WEITERE QUALIFIKATIONEN:
Clinical trial assistant
294157/11
IHRE AUFGABEN:
-Reviewing and processing of all documents received for the TMF with focus on reviewing, indexing, tracking, scanning and filing for IMP approved documents
-Ensure accurate set-up, maintenance and archiving of the TMF/eTMF within the required timeline
-Reading and QS reviewing of documents
-Support the trial management teams in the preparation, conduct, and follow up of internal and/or external audits/inspections
-Return the transmittal and confirmation of receipt (COR) of all required documents and send the COR back to the sender within the required timelines
IHRE QUALIFIKATIONEN:
-Profound administrative and clerical experience, preferably in a pharmaceutical setting
-Prior experience in working with electronic filing systems
-Strong computer skills including working Microsoft Suite
-Fluency in English
WEITERE QUALIFIKATIONEN:
Clinical trial assistant
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Sonstiges