Regulatory Submission Professional - Clinical Trial Submissions in EU

EU Submission Hub Søborg, Denmark Are you looking for an exciting opportunity where you can make a real difference? Would you like to join a dynamic international team where no two days are the same? If you thrive in a collaborative environment across cultures, this could be your next career step. Your new roleAs a Regulatory Submission Professional, you will play a critical role in managing and coordinating clinical trial submission activities within the EU. You will work in a fast-paced environment with multiple stakeholders and tight timelines, ensuring high-quality and compliant submissions.Your main responsibilities will include:Working on process optimization for CTA submissions within a team and stakeholders from other teams Working closely with various submission teams across the organization and all countries in EuropeManaging initial clinical trial application submissions in the EU according to the Clinical Trial Regulation (EU CTR) and all changes during the life cycle of cl...