About this role
Regulatory Submission Professional - Clinical Trial Submissions in EU at novonord. Location: Warsaw, Masovian Voivodeship, Poland. Role: managing submissions, coordinating responses, maintaining records Requirements: Master's in life sciences, 3+ years clinical trial/submissions experience, knowledge of EU CTR, CTIS and Veeva Vault experience preferred, strong organization and English communication skills. Category: Research and Development (R&D) Seniority: Mid Level Tools: Veeva Vault RIM, Vault Clinical (COSMOS), CTIS Commitment: Full Time Workplace: Onsite Languages: English