Italy Job Openings
IQVIA
Clinical Trial Administrator - ETMF Specialist (Italy)
Parma
FULL TIME
November 19, 2024
RESPONSIBILITIES:
- To review e TMF plans
- To upload documents in the e TMF and perform ongoing quality control of the e TMF (Investigational products and Clinical Trial Supply section) using Company System
- Monitor the e TMF quality issues and follow up with the relevant functions (internally / CMO /CRO) until their resolution.
- To provide support to e TMF 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 (DL196/2003) - General Data Protection Regulation (13 GDPR 679/16 –) to IQVIA and to transfer those data to IQVIA’s Clients. The research is urgent and is intended for candidates of both sexes (L.903/77).
#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://jobs.iqvia.com
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