SUMMARY: * Extensive medical, pharmaceutical writing, CME, sales training, promotional, regulatory, blended learning systems, and publications planning experience * Direct participation in 15 major product launches * Comprehensive regulatory /
medical affairs background * Development & «guest» writing of 26 peer - reviewed journal articles * Direct liaison with client product management, regulatory, and medical teams * Senior l...
With a strong
background in clinical research (immunoassay development, protein extraction and purification, molecular and cell biology and pharmacology), in combination with
medical and scientific writing as well as working experience with regulatory
affairs and clinical trial planning and designing, my education and experience can bring a solid foundation to the ar...