Reporting to the Manager, Case Management, the Drug Safety Specialist has the primary responsibility for the preparation and timely submission of all safety reports, including expedited safety reports. Additional duties and responsibilities...

We are seeking an innovative research candidate to be on the forefront of evaluating novel antibody drug conjugates and other candidate therapeutics in our pipeline using in vivo cancer xenograft and syngeneic tumor models. Responsibilities Primary...

Summary: Reporting to the Drug Safety Director, the PV Quality Manager is responsible for monitoring and assessing Drug Safety procedures to assure compliance with global regulatory requirements. This individual is also responsible for ensuring...

RA will work in a collaborative setting with other cell line and cell culture development staff on CMC development projects. RA’s primary responsibility is to support recombinant cell line and cell culture development. This will include recombinant...

• Perform QA reviews of analytical method validation, process validation, cleaning validation and/or shipping validation studies including reviewing protocols, executed protocols/validation data, and associated validation reports. • Provide QA...

• Perform sample size and power calculations • Review CRFs and edit checks • Develop SAP and create table, listing, and figure shells • Perform statistical analysis as defined in SAP • Able to code complex statistical analyses as needed; familiar...

Seattle Genetics is a biotechnology company advancing a broad pipeline of antibody-based therapies. In August 2011, the U.S. Food and Drug Administration (FDA) granted accelerated approval of Seattle Genetics' first commercial product, ADCETRIS™...