Scientist, Medicinal Chemistry California
1/16/2017 9:46 AM

This position contributes to and supports the company’s research and development efforts to create high value therapeutics to address unmet medical needs. The successful candidate will be responsible for: • Leading in the execution of design, synthesis, purification and characterization of bioactive compounds. • Facilitating the design of new bioactive compounds by interacting with other chemis  ...View Job
Research Associate II (In Vitro Assays/Radioligand Binding) California-San Francisco
1/16/2017 9:45 AM

Position Summary: Performs research and/or development in collaboration with others for projects. Exercises technical discretion in the execution and interpretation of experiments that contribute to project strategies. Maintains familiarity with current scientific literature. Contributes to project process within a scientific discipline. Maintains professional expertise through familiarity with  ...View Job
Director, Regulatory Affairs California
11/9/2016 3:51 PM

Responsible for oversight of all regulatory activities of regulatory team. Develops strategies for earliest possible approvals of drug applications and device registrations. Ensures appropriate project/ program Regulatory support. Provides counsel to and manages regulatory team. Participates in higher level interactions with external partners. Formulates corporate responses to regulatory agencies   ...View Job
Sr. Program Data Manager California
10/21/2016 4:18 PM

The Senior Program Data Manager independently leads the data management components of a clinical trial ranging from small early phase to large global and late phase programs. The assigned clinical trial(s) may be high complexity or high risk. The Senior Program Data Manager is accountable for ensuring study launch, conduct, and closeout are performed according to Nektar’s quality standards, Sta  ...View Job
Associate Director, Regulatory Operations California
10/21/2016 4:14 PM

Position Summary: Responsible for the management of the day-to-day Regulatory Operations functions and all submissions to Global Regulatory Authorities (i.e., FDA, EMA, etc.). This includes the development and implementation of Regulatory Operations infrastructure to support both electronic and paper submission filings, as required by Regulatory agencies. Creates processes and standard require  ...View Job