Senior RA specialist clinical trial applications
Location: NetherlandsSIRE® 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 Biotechnology organisation, based in Zuid-Holland Netherlands.
This project will take 7 months minimum. Extension is likely.
- a University degree with 4+ years of regulatory experience
- Knowledge of drug development, clinical trials and RA
- Project manager; team management experience
- Clear communicator
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.
The Company
Our client is a subsidiary of a global clinical company specialized in biopharmaceuticals.Role Description
As the manager you are responsible for making sure that regulatory requirements for clinical trials in various countries are in place. You are the head of a cross functional team and you are the point of contact for regulatory- and health authorities.This project will take 7 months minimum. Extension is likely.
Responsibilities
You lead your CTA team and make sure that applications will be compiled, published and produced. You keep track of all events regarding all regulatory aspects of clinical trials.Requirements
Your profile is a hybrid of regulatory affairs and clinical research. You have skills like:- a University degree with 4+ years of regulatory experience
- Knowledge of drug development, clinical trials and RA
- Project manager; team management experience
- Clear communicator
Other information
This position can be done by a consultant (ZZP) or through payrolling.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.
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