Clinical Research Associate in Oncology
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!
Our client is a professional Clinical Research organization, based in Netherlands.
It is the mission of the client to enhance the quality of the life via novel approaches of pharmaceuticals. In addition to that, the client strives to be a trustworthy market leader who can give significant improvement in the progression of healthcare.
Key elements of this role is to monitor and assist with the conduct of oncology trials, all in order to perform oncology research and focus on getting better or novel cancer treatments to the healthcare market
Our client has extensive experience in managing clinical trials across a range of novel anti-cancer therapies. Our client is active in multiple locations in the Netherlands and European Union and offers the opportunity to work in an national and international environment with good career prospects.
The client will give you an excellent training programme and the ability to broaden your skill set beyond that of a clinical research associate. You will have the opportunity to be involved in contributing to the development of a novel range of emerging innovative anti-cancer therapies with a broad range of pharmaceutical and biotechnology companies. This is for a full time, permanent position
-You will be based at the office located in Gelderland and travelling under optimal conditions to our clients' sites. You will monitor the clinical trials totally compliant with Good Clinical Practice rules and regulations.
-In your daily activities you will supervise the research sites to keep the data entry up to date and standardised.
-You will support and keep in close contact with clinical managers and investigators in order to improve on research outcome
-Minimal a BSc degree in life science, nursing or pharmacy equivalent degree.
-Excellent written and verbal communication skills in German (fluent/native) and English
-Motivated and able to work with little direction and with excellent attention to detail
-One to two years of experience in oncology or immunology
-Able to travel
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Hanneke de Koning.