Edison-New Brunswick Metro Area, NJ
- A MS or BS degree in a field of cell biology, biochemistry or molecular biology with 5-7 years hands-on research experience. Experience in drug discovery, oncogenic and immune cell signal transduction and translational medicine is a plus.
- Scientist specializing in cell and molecular biology supporting Translational Research by mechanism-of-action studies and defining biomarker strategies. Contributions involve expertise in enzyme and cell-based assays to the application of protein and nucleic acid technologies. Participates in activities such as vector design and generation, transient and stable cell transfection & transduction and cell-based functional assays. Experience with primary cell culture, co-cultures, flow cytometry and inducible gene silencing are a plus. Organisatorial skills, flexibility and coordination between different projects are also required.
1. Assay development to support biomarker strategies for clinical trials
2. Develop in-vitro assays for evaluating mechanisms of drug resistance, drug differentiation and pharmacodynamic marker identification (develop resistant cell lines, make stable and conditional knock-downs and knock-ins, cellular trafficking studies)
3. Study the intracellular signaling networks and feedback mechanisms within pertinent cell types to assess mechanism of action and rationalize drug combination strategy.
4. Interface with bioinformaticians to analyze genomics data for understanding pathways of resistance and differentiation o drugs in development
5. Participate in translational team meetings to present data and provide interpretation
6. Analyze, interpret, and present experimental results.
7. Ensures that the Translational Development Department maintains current awareness in area of expertise, enhances the scientific credibility through contributions to the scientific literature (publications/presentations), through extramural activities and scientifically related interactions with academics
8. Contributes to bringing new technologies in-house
9. Assumes responsibility for writing non-clinical pharmacology study reports, invention disclosures, and contribute to the writing of investigator brochures, IND applications, regulatory annual reports, and other regulatory documents when appropriate.