Safety & PV Submission Spec I

This position is listed on behalf of a partner company, which manages all applications and next steps. Our partner is looking for a Safety & PV Submission Spec I based in Brazil.
In this role, you will support the preparation, coordination, and submission of critical pharmacovigilance and drug safety reports to regulatory authorities, ethics committees, and clinical investigators. You will contribute to ensuring that safety documentation is accurate, complete, and submitted within established regulatory timelines. Working within an international clinical research and life sciences environment, you will collaborate with internal project teams, clients, and external stakeholders to support clinical trials and post-marketing safety programs. You will help maintain submission records, organize essential documentation, and ensure compliance with applicable regulatory requirements and industry standards. This position offers an opportunity to develop your expertise in pharmacovigilance, clinical research, and regulatory safety reporting while contributing to processes that support patient safety. The ideal candidate is detail-oriented, organized, and comfortable managing multiple priorities in a collaborative, quality-focused environment.

Skills
Clinical Research, Pharmacovigilance, Documentation

Employment type
Full-time

Work arrangement
Yes