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Registration Officer Freelance

SIRE Life Sciences®

Netherlands, zagranica

SIRE Life Sciences®

Registration Officer Freelance

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 Noord-Brabant Netherlands.

Caring for the world, one person at a time’... inspires and unites the people of our client. They embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people.

ROLE DESCRIPTION

In order to support this multinational their registration process they are looking for a freelance professional that can work the eCTD processes.

RESPONSIBILITIES

Work with a team of three publishers; trained on all aspects of publishing and submission processing, including setting and tracking timelines, electronic submission preparation and RA, and eCTD compilation.
* System/process owner of SharePoint (for AIP program for document sharing and collaboration), Documentum, CoreDossier, and eCTD.
* Led the development, refinement and rollout of internal guidelines, procedures and processes pertaining to submission building
* Support the liaising across departments and with external partners on submission strategy by the RA manager;
* Support outsourcing of publishing during transition to hosted environment of eCTD.

REQUIREMENTS

Regulatory Operations professional with a technical knowledge of R&D applications and a successful track record of leading projects and initiatives directly supporting corporate objectives.
* Hands-on experience with Regulatory Affairs submissions
* Adept at following guidelines and procedures and project documentation

Computer Skills
* eCTD
* SharePoint
* Adobe Acrobat Professional
* MS Office

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

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

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