About Jeffrey Autrey
jeffreyautrey.blogspot.com/jeffreyautrey.blogspot.com/Jeffrey Autrey has spent over 16 years in the pharmaceutical industry, during which he has served as a submission manager. In 2004, Jeffrey Autrey joined Pfizer as a US Hub Submission Manager.
Early in his career, he was a dedicated resource to content contributors and provided support for US lifecycle submissions. Alongside clinical compliance tracking, he was responsible for toxicology support review cycles and related data entry duties.
Later on, Jeffrey Autrey began a new role as a global submission manager. Working with product teams and clients, he oversees regulatory operations activities and standards associated with major product submissions.
For his work on Bavencio’s US drug submissions, Jeffrey Autrey received the Saxton Clinical Development Large Team Award on two occasions.
A graduate of Temple University, he has a master’s degree in quality assurance and regulatory affairs, and enjoys keeping up with new procedural and technical developments within submission management science and the expansion of eCTD format standards around the globe.
Early in his career, he was a dedicated resource to content contributors and provided support for US lifecycle submissions. Alongside clinical compliance tracking, he was responsible for toxicology support review cycles and related data entry duties.
Later on, Jeffrey Autrey began a new role as a global submission manager. Working with product teams and clients, he oversees regulatory operations activities and standards associated with major product submissions.
For his work on Bavencio’s US drug submissions, Jeffrey Autrey received the Saxton Clinical Development Large Team Award on two occasions.
A graduate of Temple University, he has a master’s degree in quality assurance and regulatory affairs, and enjoys keeping up with new procedural and technical developments within submission management science and the expansion of eCTD format standards around the globe.