Ying Zhang Email & Phone Number | I am a Ph.D. Biostatistician supporting all stages of oncology and rare disease clinical trials, and an experienced program lead and people manager with good communication skills. Practical experience in clinical trial design/simulation, protocol, statistical analysis plans (SAPs) and TFL shell development/review to ensure high quality data analysis. Extensive experience in managing internal and CRO project activities including timelines, deliverables. Ensures achievement of major statistical deliverables and milestones in coordination with other functions. Proficient programming skills in SAS (macro), R, SQL, EAST, Seamless R and C++ integration. Knowledgeable in CDISC standards and disease areas under study (e.g. endpoints, available treatments, course of disease and primary analysis).

Ying Zhang

I am a Ph.D. Biostatistician supporting all stages of oncology and rare disease clinical trials, and...
San Francisco Bay Area, San Francisco Bay Area, United States

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Ying Zhang’s Email yzhang@ascendispharma.com

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Ying Zhang’s Location San Francisco Bay Area, San Francisco Bay Area, United States

Ying Zhang’s Current Industry Ascendis Pharma

Ying Zhang’s Prior Industry Ultragenyx Pharmaceutical | Novartis | Allergan | Genentech

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Work Experience

Ascendis Pharma

Director Biostatistics

2022-01-01T00:00:00.000Z - Present

Ultragenyx Pharmaceutical

Senior Manager, Biostatistics

2017-01-01T00:00:00.000Z - 2019-01-01T00:00:00.000Z

Novartis

Principal Biostatistician

2016-01-01T00:00:00.000Z - 2017-01-01T00:00:00.000Z

Allergan

Intern

2015-01-01T00:00:00.000Z - 2015-05-01T00:00:00.000Z

Genentech

Summer Intern

2015-01-01T00:00:00.000Z - 2015-01-01T00:00:00.000Z

Skills

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Languages

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FAQ About Ying Zhang

Ying Zhang is located at
San Francisco Bay Area, San Francisco Bay Area, United States

Ying Zhang is a I am a Ph.D. Biostatistician supporting all stages of oncology and rare disease clinical trials, and an experienced program lead and people manager with good communication skills. Practical experience in clinical trial design/simulation, protocol, statistical analysis plans (SAPs) and TFL shell development/review to ensure high quality data analysis. Extensive experience in managing internal and CRO project activities including timelines, deliverables. Ensures achievement of major statistical deliverables and milestones in coordination with other functions. Proficient programming skills in SAS (macro), R, SQL, EAST, Seamless R and C++ integration. Knowledgeable in CDISC standards and disease areas under study (e.g. endpoints, available treatments, course of disease and primary analysis).