I’m the Practice Lead for Regulatory Affairs and Medical Writing for the Ascent Life Science Division and have more than 10 years of active and passive contract and permanent recruiting in the spectrum of clinical development and pre-clinical space for Pharmaceutical, Biotechnology, Medical Device, Diagnostic, Clinical Research Organizations and Consulting firms for North America.
My specialties have become Regulatory Affairs, Drug Safety and Medical Writing (Regulatory & Publications), but I also cover Medical Information/Communications, Drug Development Project Management, Medical Affairs, Health HEOR/Epidemiology and Clinical Quality.
I have my finger on the pulse of the industry and know what’s hot and what’s not and love talking with highly educated people that share my same passion. I grew up a military brat and lived in both Europe and Asia. My exposure to different cultures and prior experience working at a source plasma collection center in industry has prepared me for the global world of drug development.
If I don’t work in your space, just ask me to connect you to someone at Ascent that does.
Please reach me at 303-694-5482.
Feel free to add me to your LinkedIn network https://www.linkedin.com/in/lindseysummers, join my group on the Changing FDA Regulatory Landscape in the United States https://www.linkedin.com/groups/12041300 and follow me on Twitter @biopharmasleuth.