A qualified professional with regulatory expertise and experience gained within the global pharmaceutical, regulatory, hospital pharmacy and clinical research industry. I have experience in the preparation, co-ordination and review of various scientific and regulatory documents for UK, Ireland, European and Eastern European countries. I am a self-motivated and hard working individual with a very flexible and open style, with excellent verbal and written communication skills, which enables me to relate with a wide range of people from different backgrounds. I am a keen team player and can also work well independently without supervision. I'm success driven and enjoy the challenges of the regulatory environment within the pharmaceutical development arena. I have strong problem solving skills, have effective time management skills and I am focused and pay attention to detail. I am dedicated to maintaining high quality standard, and to achieve deliverable results. I am proficient in the use of IT packages such as Word and Excel. Overall my goals are to contribute to my employers’ profitability through my determination to succeed in my working environment.
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