Sr. Biologist ( Molecular Profiling)

Dear Candidate,

We at MAKRO deliver custom client-centric solutions by offering contract outsourcing and premium staffing to the most well known life sciences organizations throughout the United States. Our broad geographic reach, scalability and immense talent pool enable us to reliably meet the needs of our esteemed clients.

We thoroughly understand and believe that long lasting in-depth relationships with clients is an integral part in the business environment and equally important is the relationship with our candidates.

Our vision is to become a most reliable 'connector' between Pharmaceutical, Biotechnology, Medical Device companies and Best Talent.

Job Title:  Sr. Biologist ( Molecular Profiling)

Location: Westpoint,PA

Duration : 12 Months contract

Full Requirement : 

Qualifications:

·         Ph.D. and/or M.D. plus at least two years post-doctoral experience required.

·         Experience must include application of Molecular Profiling technologies, analysis and interpretation of large microarray or gene expression data sets.

·         Direct experience with clinical development, toxicogenomics, RNA therapeutics and strong statistical skills preferred.

Responsibilities:

·         This position, which will be based at Client's research facility in West Point, PA, will have the following primary responsibilities:

·         collaborate with basic research, pre-clinical, and clinical scientists to design studies that heavily leverage MP technologies, with a primary emphasis on RNA profiling but also including genotyping, deep sequencing, proteomics and metabolomics

·         Integrate data from internal experiments with data in the public domain for biomarker and target discovery

·         Translate the results from MP studies to concrete deliverables that enable the CLIENT drug discovery and development pipeline, and collaborate with statisticians and bench scientists to develop robust clinical biomarker assays

·         Contribute biomarker sections to clinical development plans and clinical protocols

·         Leverage MP technologies to provide novel readouts that can help maximize the development of RNA therapeutics and drug toxicity components

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