Manager, Medical Writing California-San Francisco
11/19/2015 5:10 PM

Responsible for supporting CRAs and MDs in clinical protocol development, Investigator's Brochures, informed consents and INDs/IMPDs. Responsible for researching, writing and editing clinical reports, summarizing data from clinical studies for submissions to the FDA and for publication and/or presentation. Will also contribute to the development of formats medical writing infrastructure. Remains   ...View Job
Manager, GCP Compliance California-San Francisco
11/19/2015 5:00 PM

Position Summary The Manager of GCP Compliance leads and directs GCP compliance activities that primarily support the Development Organization. The position helps ensure GCP compliance by assisting with the development and implementation of Clinical Developmentā€™s quality system and processes. This includes helping establish and implement quality standards, conducting internal and external audit  ...View Job
Executive Director, Drug Safety (MD) California-San Francisco
11/19/2015 4:50 PM

Overall responsibility for leading the Drug Safety Team and directing the safety surveillance of all company investigational drug products in development and for managing patient safety and meeting regulatory reporting requirements. Actively participates in the oversight of patient safety in all on-going clinical trials. Directs and conducts ongoing safety surveillance of company drug products.   ...View Job