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Company

ClinChoice · 1 day ago

Senior Statistician Consultant (Remote)

United States

Full-time

Remote

Mid, Senior Level

2+ years exp

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BiotechnologyConsulting

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Responsibilities

Responsible for protocol development including study design, sample size calculation, randomization, and statistical analysis plan for assigned studies.

Provide statistical oversight to studies and assure adequate quality and consistency with project requirements.

Responsible for assuring that data for statistical analyses are complete, accurate and consistent.

Responsible for statistical analysis plans and the accuracy and timeliness of statistical input into reports or decisions.

Responsible for validity of analysis and explore alternative analysis strategies as needed.

Demonstrates extensive understanding of statistical concepts and methodologies. Recognizes and corrects flaws in scientific reasoning and statistical interpretation.

Responsible for accuracy and consistency of statistical tables, figures, and data listings, accuracy of report text, and consistency between summary tables in the body of reports and the corresponding source tables and listings.

Responsible for statistical methods section for the reports. Identifies and corrects common flaws in interpretation of results, inconsistency in presentation or inference, adherence to the report guidelines, and assures project-wide consistency.

Effectively mentor peers with regards to statistical methodology and provide appropriate training to less experienced statisticians.

Manage activities of statisticians across projects by appropriately coordinating assignments and reviewing work so that projects are delivered on time with high quality.

Qualification

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MSStatisticsSAS skillsStatistical analysis planStatisticsPharmaceutical industry experienceClinical trials experienceFDA regulations knowledgeData interpretationStudy designMentoring skills

Required

MS or PhD in Statistics, Biostatistics or related field. PhD with 2-4 years of experience or MS with 5-7 years of experience

Strong SAS skills

Interpretation of data for internal team (clinical, stats,..)

Working on study readouts ( AKA) analysis results from Tables listings and figures

Strong oral and written communications skills, with ability to effectively communicate internally and with clients

Demonstrated understanding and insight in statistics, drug development process and relevant FDA regulations

Pharmaceutical, CRO, or related industry experience with clinical trials, including interaction with Regulatory Agencies, especially FDA

Company

ClinChoice

Glassdoor

3.7

ClinChoice is a full-service global clinical CRO dedicated to offering high-quality, efficient and flexible solutions to pharmaceutical, biotechnology, medical device, and consumer products clients worldwide.

Founded in 1995

Shanghai, Shanghai, CHN

1,001-5,000 employees