Roche

88-50100571 Analytical Data Scientist

Roche$142K — $197K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Master's degree in biostatistics, mathematics, data science or closely related field required.
  • Proven experience in statistical programming for clinical and biomedical data.
  • Expertise in SAS, SQL, and R for software development and programming.
  • Solid understanding of statistical methodologies such as survival modeling, causal inference, and clinical trials.
  • Experience collaborating with diverse stakeholders in biomedical research projects.

Responsibilities

  • Conduct statistical programming and analyses for drug development within a global biotech organization.
  • Lead teams in planning and implementing statistical software solutions for clinical trial reporting.
  • Develop and validate datasets and statistical outputs for clinical studies including SDTM and ADaM datasets.
  • Communicate with interdisciplinary stakeholders to negotiate project timelines and deliverables.
  • Identify and delegate deliverables for clinical study team members to support various programs and studies.
  • Assist in creating visualizations and dashboards for data exploration and insights.
  • Resolve technical issues in coding or outputs and ensure data integrity.

Benefits

  • Flexible work-from-home policy allows for telecommuting up to 3 days a week.
  • Part of a global health authority collaboration to support product pipelines.
  • Access to comprehensive learning and development opportunities.
  • Participation in a discretionary annual bonus based on performance.
  • Collaboration with diverse scientific teams across the organization.
Full Job Description
The Position

Genentech, Inc. seeks an Analytical Data Scientist at its South San Francisco, California location.

Duties: Within global biotechnology organization, conduct statistical programming and analyses to support the company's Product Development Data (PDD) Sciences used for pharmaceutical and biotech drug development. Lead statistical programming teams in planning, designing, and implementing statistical software solutions for clinical trial reporting and analysis. Assess, clarify and make statistical recommendations on study requirements, develop statistical programming strategies, and ensure efficient implementation as the Study Lead. Develop data science strategies to meet study and project requirements; manage output specifications and output risk assessments; and specify, review, and implement analysis datasets. Identify and assign deliverables for clinical study team members in support of across molecule programs. Conduct statistical programming and analytics as a component of clinical projects. Communicate with stakeholders from different scientific backgrounds and areas of expertise to negotiate timelines and scope of deliverables. Develop and validate datasets and statistical outputs for clinical studies, including Study Data Tabulation Model (SDTM) datasets, Analysis Data Model (ADaM) datasets, and tables, listings, and figures (TLFs) through adherence to risk assessment and quality control guidelines and internal processes. Assist in developing visualizations/dashboards for data exploration using interactive applications and data insights platforms. Document reproducible and accurate outputs and ensure alignment with programming specifications. Resolve technical issues in code or output that cause data discrepancies. Collaborate with global health authorities to support company's product pipeline and build partnerships to collaborate with global affiliates to support products, processes, and systems while ensuring compliance with regulatory and process requirements.

Education and Experience Requirement: Requires a Master's degree in biostatistics, mathematics, data science or closely related field.

Specials Skills Requirement: Must have the following skills from academic studies, research, or industry: 1) Statistical programming knowledge of clinical and biomedical data in product development processes within biopharmaceutical industry, 2) Software development and programming expertise in SAS, SQL, and R, 3) Statistical methodologies in biomedicine such as survival modeling, causal inference, and clinical trials, and 4) Collaborating with stakeholders from different scientific backgrounds on biomedical related research projects. May telecommute up to 3 days per week.

#LI-DNI #DNI #DE-DNI

Worksite: 1 DNA Way, Central Campus, South San Francisco, California 94080.

The expected annual salary range for this position based on the primary location for this position in South Francisco, California is $142,656 to $197,500 per year. Actual pay within the range will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at

(https://roche.ehr.com/default.ashx?CLASSNAME=splash).

About Roche

Roche Holding AG is a Swiss multinational healthcare company that operates worldwide under two divisions: Pharmaceuticals and Diagnostics. Its holding company, Roche Holding AG, has bearer shares listed on the SIX Swiss Exchange. The company headquarters are located in Basel. Roche is the largest pharmaceutical company in the world, and the leading provider of cancer treatments globally. The company also produces a range of diagnostic tests for medical professionals and patients. Roche was one of the first companies to bring targeted treatments to patients. In 2019, Roche had over 100,000 employees worldwide, and generated revenue of CHF 61.5 billion.
Learn more about Roche
Size
100,920 employees
Industry
NASDAQ

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