Global Regulatory Specialist
8 godzin temu
We are a global Big Pharma company offering a stable job environment, international team, benefits package, and hybrid or remote work options. As a Global Regulatory Specialist, you will have the opportunity to work on complex regulatory projects, collaborating with regional and global teams. Our goal is to provide job seekers with new opportunities, helping them find employment that matches their qualifications and experience.
Responsibilities:- Regulatory Strategy Development: Develop and implement regulatory strategies to optimize product development and commercialization
- Stakeholder Engagement: Foster strong relationships with regional stakeholders and LOCs, driving alignment between regional and global strategies
- Process Improvement: Lead the development of streamlined regulatory submission processes and ensure meticulous review and management of regulatory documents
- Clinical Trial Management: Manage the assembly and submission of clinical trial applications, ensuring seamless execution of regulatory requirements
- Marketing Authorization Support: Play a pivotal role in supporting registration processes and maintaining dossier readiness
- Degree: Bachelor's Degree in Pharmacy, Chemistry, Medicine, or Biotechnology
- Experience: 2+ years of experience in regulatory affairs within the pharmaceutical industry
- Knowledge: General understanding of the pharmaceutical industry and regulatory environment in drug development and/or marketed products
- Skills: Strong analytical and problem-solving skills, with attention to detail and exceptional organizational skills
- Job Environment: Stable job environment
- Team: International team
- Benefits: Benefits package
- Work Options: Hybrid or remote work options
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