Tim W

Tim W has extensive work experience in the pharmaceutical industry. Tim began their career at Biogen Idec, Inc. in 2002, where they worked as a Specialist in Medical Information and Communications. Tim then transitioned to the role of Sr. Analyst in Medical Affairs Oncology. In 2006, they worked as a Technical Writer at Genentech. From 2007 to 2009, Tim held the position of Clinical QC Associate II, Medical Writing at Amylin Pharmaceuticals. Tim then joined NuVasive as a Medical Writer Consultant from 2009 to 2011. Tim then moved on to Optimer Pharmaceuticals, where they worked as a Regulatory Review Specialist and later as a Regulatory Review Specialist Consultant. Since 2014, they have been employed at Acadia Pharmaceuticals Inc., starting as a Regulatory Document Quality Specialist (Consultant) and progressing to the roles of Regulatory Document Quality Specialist, Regulatory Document QC Manager, Sr. Regulatory Document QC Manager, and currently, Associate Director of Regulatory Document QC.

Tim W has a BSc degree in Biological Sciences from The University of Edinburgh.