Willing to relocate: No, but I am open to discussing a reasonable schedule of visiting HQ/my team's office (e.g. once a quarter for a week)
Primary expertise and experience: Solution development, value proposition development, cross-functional & multinational team collaboration and management, FDA regulatory affairs (with EMA and PMDA familiarity), project management, stakeholder management
Résumé/CV: Please email me for a .pdf of my CV
Email: dyhndz [at] gmail [dot] com
LinkedIn: www.linkedin.com/in/dyhndz
Hi, I am a highly motivated biotechnology professional with a diverse experience background including time at a top 10 global pharma company, national government laboratory, rare disease biotech startup, and now international CRO. I also have a graduate level academic background in biochemistry. I have collaborated with cross-functional teams and subject matter experts to develop product regulatory development support solutions and value propositions for over 160 biotech and 5 international pharmaceutical companies.
My goal is to take my experience developing support solutions for drug and medical device sponsors and apply it by working for a sponsor or other company directly, utilizing my end-to-end drug development and regulatory knowledge as well as solution development and management expertise to contribute to the company's mission. I am also interested in & open to roles within the tech/SaaS space, among a variety of others that employ any of my listed skills. Thanks!
Remote: Yes
Willing to relocate: No, but I am open to discussing a reasonable schedule of visiting HQ/my team's office (e.g. once a quarter for a week)
Primary expertise and experience: Solution development, value proposition development, cross-functional & multinational team collaboration and management, FDA regulatory affairs (with EMA and PMDA familiarity), project management, stakeholder management
Résumé/CV: Please email me for a .pdf of my CV
Email: dyhndz [at] gmail [dot] com
LinkedIn: www.linkedin.com/in/dyhndz
Hi, I am a highly motivated biotechnology professional with a diverse experience background including time at a top 10 global pharma company, national government laboratory, rare disease biotech startup, and now international CRO. I also have a graduate level academic background in biochemistry. I have collaborated with cross-functional teams and subject matter experts to develop product regulatory development support solutions and value propositions for over 160 biotech and 5 international pharmaceutical companies.
My goal is to take my experience developing support solutions for drug and medical device sponsors and apply it by working for a sponsor or other company directly, utilizing my end-to-end drug development and regulatory knowledge as well as solution development and management expertise to contribute to the company's mission. I am also interested in & open to roles within the tech/SaaS space, among a variety of others that employ any of my listed skills. Thanks!