My background includes 13 years’ experience in the Pharmaceutical Industry at AstraZeneca Pharmaceuticals in Global Regulatory Submissions and Life Cycle Management of Regulatory documents. This includes 6 years’ experience as a Project Manager for Regulatory Global submissions. As a Project manager within the Submission Management Group, I provided expertise on global submission compilation and published electronic submissions compiled in RSS Application in accordance with Health Authority guidelines and departmental standards. I have coordinated all submission activities with Regulatory Global Leads and Marketing Companies to ensure quality submissions met and/or exceeded Health Authorities expectations for approvals.

Highlights:

• Newark, DE
• Life Cycle Management
• Regulatory Global Submissions
• Pharmaceutical Industry
• RSS Application
• eCTD Publisher
• electronic submissions
• Regulatory Publisher
• Management
• Cardiovascular
• Document Management
• Legal
• Pharmaceutical
• Project Management
• Publishing
• Quality Assurance