Research staff Prestige Biopharma
• Focus on regulatory affairs. Works closely with our team to ensure that all of our research and development activities are in compliance with relevant regulations and guidelines.
• Editing and reviewing Standard Operating Procedures (SOPs), Manuscripts, and Study Reports ensuring that they are accurate, complete, and compliant with regulatory requirements. This involves collaborating with colleagues from various departments and using attention to detail and strong editing skills to ensure that all documents are of the highest quality.
• Assist with regulatory submissions, including compiling necessary documentation and ensuring that submissions are submitted on time and in compliance with relevant regulations. Responsible for maintaining accurate and up-to-date records of all regulatory-related activities.