Manufacturing Associate California
4/22/2017 10:41 AM

A privately held, emerging molecular diagnostics company in the Bay Area has a opportunity for a Manufacturing Associate. The company’s testing product line, is a PCR based product used in organ and stem cell transplantation and other areas of immunogenetics research. The manufacturing associate will produce and assemble our proprietary and leading edge molecular diagnostics products. The succ  ...View Job
Research Associate California
4/6/2017 1:06 PM

Primarily be responsible for developing and performing binding assays, kinetic profiling assays, competition assays, efficacy assays and epitope binning of early therapeutic candidates using a wide range of biophysical and biochemical methods including Biacore, MASS-1, Octet, FRET, ELISA, etc.  Implement and validate protocols.  Reviewing literature for technical support.  Data analysis.  With  ...View Job
Biologist - Drug Discovery California
3/15/2017 1:56 PM

DUTIES: • Design appropriate assay protocols for the projects. • Identify CRO and external labs for conducting the needed studies and oversee contracted studies. • Manage outside collaborations. • Organize, record and report results to project team. • Ensure complete data and other records into internal databases. • Be responsible for all biological aspects for assigned drug discovery   ...View Job
Scientist, Clinical Pharmacology California
2/21/2017 12:02 PM

RESPONSIBILITIES • Design and interpret PK/PD studies in support of molecules in clinical and nonclinical development • Analyze, Model, simulate and predict nonclinical and clinical data to drive decisions on dose and frequency of • dosing • Perform population PK and PK/PD analyses on drug candidates as they progress through clinical development • Interact with pharmacologists, toxicologists  ...View Job
Clinical Trial Manager California-Silicon Valley/Peninsula
2/21/2017 12:02 PM

One of our biopharmaceutical clients is recruiting for a Clinical Trial Manager. - Manage clinical trial outsourcing by developing an outsourcing strategy for specific elements of the trial, identifying and selecting CROs, and managing CRO performance - Review and contribute to study documentation including informed consent templates, protocols, case report forms, source documents, study plans,   ...View Job