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Data management and quality assurance specialist

Livorno
beBee Careers
Pubblicato il Pubblicato 10h fa
Descrizione

Job Title: Data Management Specialist


Description:

We are seeking an experienced Data Management Specialist to oversee data management and statistics trial documentation in accordance with internal standards and regulatory requirements.

The successful candidate will be responsible for ensuring TMF documentation is published in a timely manner and with high quality, maintaining TMF in an inspection and audit readiness.

You will lead the Documentation and Data Archiving team, providing subject matter expertise and guidance to team members.

* To ensure providers match performance expectations
* To promote optimal use of tools and metrics related to documentation management

This role requires strong knowledge of clinical data management and statistical processes, as well as international standards for Trial Master File (TMF Reference Model) and ICH GCP and regulatory requirements.

The ideal candidate will have a scientific degree, significant experience in a similar job in the industry or CRO, and excellent communication skills.


Responsibilities:

* Lead the documentation and data archiving team, recruiting, mentoring and developing the team
* Train DM/STAT CRO on Company standards and TMF related activity
* Monitor TMF related activities using metrics to evaluate status and gaps to ensure quality and timelines and evaluate corrective actions
* Support team members in the TMF plan activities and quality checks
* Participate to audit and inspection to TMF
* Perform regular checks on data archiving activities to ensure timelines are respected
* Contribute to eTMF process improvement and internal system development


Requirements and Skills:

* Scientific degree
* A significant experience in a similar job in the industry or CRO
* Knowledge of drug development process
* Solid knowledge of clinical data management and statistical process and related documentation, standards and tools
* Strong knowledge of international standards for Trial Master File (TMF Reference Model)
* Knowledge of ICH GCP and regulatory requirements with specific reference to data integrity, data archiving and document management
* Good knowledge of SAS System
* Knowledge of international data standards (CDISC) and regulatory requirements for data submission
* Project and budget management
* English knowledge

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