Regulatory Affairs Specialist
Yesterday
Description
• Responsible for the day-to-day activities and delivery of Global Regulatory Affairs support services. • Role will include management of clinical trial applications to Competent Authorities, Ethics Committees and Regulatory Agencies. • Develop stakeholder tools, process/document regulatory risk assessments, and provide support and expertise. • Ensure high quality, timely service delivery processes in accordance with corporate, industry and regulatory standards. • May be required to coach peers and/or provide input for staff performance reviews.
Requirements
• Applicants should have a minimum of an undergraduate degree and 4-6 years of relevant experience in Clinical Research/Regulatory Affairs. • The successful candidate will possess strong knowledge of EMA regulations.
Benefits
• Home-based • Accommodations for job applicants with disabilities are available upon request.
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