CLINICAL TRIAL ADMINISTRATOR - ETMF SPECIALIST (ITALY)
Descrizione dell'offerta di lavoro
RESPONSIBILITIES.
To review eTMF plans To upload documents in the eTMF and perform ongoing quality control of the eTMF (Investigational products and Clinical Trial Supply section) using Company System Monitor the eTMF quality issues and follow up with the relevant functions (internally \/ CMO \/CRO) until their resolution.
To provide support to eTMF users (CMOs) on the use of the system.
Archiving of study CTS related documentation in the Company CTS repository Support to collect the CTS documentation for CTA application REQUIREMENTS AND SKILLS.
High School and\/or College Degree A significant experience in a similar job in the industry or CRO Knowledge of drug development process English knowledge Solid knowledge of clinical data management and Problem solving English Proficient TYPE OF CONTRACT.
Maternity replacement IQVIA reserves the right to evaluate candidates with domicile \/ residence and work experience \/ study with requirements responding to the open request.
Applications WITHOUT the requirements Will NOT be fully taken into account.
Please enter the authorization for the processing of personal data (DL) - General Data Protection Regulation (13 GDPR -) to IQVIA and to transfer those data to IQVIA's Clients.
The research is urgent and is intended for candidates of both sexes (L.).
#LI-CES #LI-DNP IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
Learn more at https.
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Dettagli dell'offerta
- Imprecisato
- 20/11/2024
- 18/02/2025
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