Freelance RA Manager
Location: BelgiumSIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences 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!Our client is a professional Pharmaceutical and Biotechnology organisation, based in Oost-Vlaanderen Belgium.
- Providing product information
- Ensuring that reviews are conducted properly
- Ensuring that the regulatory submissions are followed up and that the system is updated
- Communicate and cooperate with external and internal stakeholders on all levels
- Ability to make priorities
- Good presentation skills
- Bachelor degree
- Experience within a pharmaceutical or biotech industry
- Experience with European MAAs.
- Experience within regulatory legislation
- Good written and verbal skills in English and Dutch
The Company
Our client is a professional Biotechnology and Pharmaceutical organization, based in Oost-Vlaanderen Belgium. The company uses medical and scientific expertise in all phases of the lifecycle of their products, continuing the growth of their company.Role Description
As a self-employed regulatory affairs officer you will be occupied in the preparation of regulatory submission and make sure that these are followed up and updated in the system.Responsibilities
- Accountable for the making of regulatory submissions- Providing product information
- Ensuring that reviews are conducted properly
- Ensuring that the regulatory submissions are followed up and that the system is updated
- Communicate and cooperate with external and internal stakeholders on all levels
Requirements
- Knowledge of both local and European labelling + Middle East big plus- Ability to make priorities
- Good presentation skills
- Bachelor degree
- Experience within a pharmaceutical or biotech industry
- Experience with European MAAs.
- Experience within regulatory legislation
- Good written and verbal skills in English and Dutch
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