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Freelance RA specialist eCTD

SIRE Life Sciences®

Netherlands, zagranica

SIRE Life Sciences®

Freelance RA specialist eCTD

Location: Netherlands

SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!

THE COMPANY

Our client is a professional Pharmaceutical organization, based in Utrecht Netherlands.

Our client is a global pharmaceutical company.

ROLE DESCRIPTION

This role has been created to get a large eCTD-project started. You will be part of an RIMS project to get the diverse regulatory affairs department ready to make the transfer towards the eCTD program. This project will take up to 6 months with the possibility to get prolonged if there are more tasks that need your expertise. The project will be full time on-site but occasional homebased work will be possible.

You will report to the RA project manager.

RESPONSIBILITIES

You will be required to help set up the data system to prepare for the datamigration towards the eCTD program. Your experience on a RA department and your knowledge of RA document setup will be an asset to your design and implementation of the system. It is your goal to create the platform that facilitates the data migration, make sure that all applications within the various departments are integrated and work fluently.

REQUIREMENTS

- A degree in pharmaceutics or chemistry
- Experience on a pharmaceutical Regulatory Affairs department and average CTD-knowledge
- Experience with eCTD-tools, system documentation
- MS office
- Organized personality

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Naut van Osnabrugge.

Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
SIRE Life Sciences®

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