Regulatory Professional - Clinical Trial Submissions in EU

Job description

Research & Development Soeborg, Denmark: Are you looking for something new and exciting, a job where you could make a difference? Do you want to join a team where action never stops, and every day never looks the same? Do you love working in international environment surrounded by people with different backgrounds and cultures? We are seeking a highly qualified individual to join our team – Regulatory Professional. Apply today and join a newly established virtual team – with colleagues in Denmark, Poland and India - focusing on clinical trial submissions in EU. Your new role: As Regulatory Professional, you will play a crucial role in driving, coordinating, and actively following up on multiple tasks with challenging timelines. Your responsibilities will include: The complexity of the tasks will be tailored to the candidate’s level of experience. - Working on process optimisation for CTA submissions within a team and stakeholders from other teams. - Working closely with various submission teams across the organization and all countries in Europe - Managing initial clinical trial application submissions in the EU according to the Clinical Trial Regulation (EU CTR) and all changes du...