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SUMMARY Over 20 years Pharmaceutical and Biotechnical Experience in Regulatory Affairs, Regulatory Operations, Clinical Regulatory Affairs, and Electronic Data Management Systems New Drug Applications, Investigational New Drug Applications, Clinical Trial Applications Specializing in IND and CTA submissions approvals and maintenance
i have kids an wanna do right by them need to advance my self to show people i can do more in life
I am a certified PMP Project Manager with 19 years of project manager experience; the bulk of my career is in software development. Most recently, I worked at Alcon Labs as a development manager where I was responsible for managing the daily activities of 5 software developers and 2 verification engineers; managing the development of up to 14 software projects simultaneously; and functionally managing a group of 15 so...
To pursue a challenging career in Drug Regulatory Affairs and become a part of an esteemed organization where I can use my skills, understanding and experience to bring out the best results and contribute to the growth of the organization.