REGULATORY
I am a Medical Doctor with more than 25 years of experience in the Pharmaceutical Industry. Until the year 2011, I worked in different CRO in various positions, and I finished my corporation career as a Global Project Manager at PAREXEL. During that time, I had a chance to gain most of the skills you list in your proposal. I do not b think there is a place here to confirm it one by others.
In 2011, I started my own company - MedRes - dedicated to regulatory and scientific (communication) Medical Writing. I attach my professional CV, will you be interested in particular works, please let me know, and I will send you my portfolio.
I am an open and straightforward person. Not only that, but I like to work in teams (please note for many times I was a PM). I like learning new things (I have just started my PhD in medicine this year). I can, and I do deliver work on time, without delays.
Furthermore, I am a member of several Intentional associations and activities, which helps me to be still informed on new issues in the MW field as well as deliver my work prepared as state-of-the-art.
I will be happy if I could present myself to you in more detail in a phone interview. I do believe I can be of an asset for your organization and the team.
I am looking forward to hearing from you soon.
With kind regards.
Marcin Dudek