Daiichi Sankyo and its 15.000 employees in more than 20 countries are dedicated to the creation and supply of innovative pharmaceutical products. In addition to a strong portfolio of medicines for cardiovascular diseases, under the Group’s 2025 vision to become a “Global Pharma Innovator with Competitive Advantage in Oncology,” Daiichi Sankyo is primarily focused on providing novel therapies in oncology. Our European headquarters are in Munich, Germany and we have affiliates in 13 European countries including Denmark, where Copenhagen acts as the Nordic headquarter.
For our headquarter in Munich we are seeking highly qualified candidates to fill the position:
Regulatory Affairs - Clinical Trial Support (m/f/x)
To serve as the European regulatory coordinator and support for assigned projects, products and non-project work in the area of Clinical Trials. Represent Regulatory Affairs internally working on a collaborative basis both within Europe and globally to become a fully recognized support function of clinical study teams and relevant stakeholder, provi ding support to EU regulatory strategists. Represent Regulatory Affairs working with authorities, affiliates, partners and CROs).
Role and Responsibilities:
We offer an interesting, diversified and challenging position, good contractual conditions, flexible working models, all the social benefits of a modern company and a professional environment where you will have the opportunity for personal growth.