Senior To Associate Director, Biostatistics

Penfield Search Partners, San Rafael, CA (United States)

Category: Programming

Posted on: 20 Nov 2020

Job Description

Our client is a leader in the development of first-in-class, innovative medicines for the treatment of various chronic and debilitating diseases across several therapeutic areas. The products they develop span not only specific indications but represent a broader platform that enable them to investigate pathways and mediators that are central to multiple diseases. Currently they are seeking an experienced Statistician to join its stable and well-staffed Clinical Development team.  This diverse pipeline of drug discovery, clinical development, and commercialization programs exist across multiple jurisdictions, including Europe, China and Japan. They also have strategic partnerships that further expand their global reach. The level of this role is flexible, and can come in anywhere from the Senior Biostatistician to the Associate Director level.

In this role you will:

    Provide sound experimental design and data analysis expertiseAuthor the protocol statistical sections and generate statistical analysis plans and study randomizationReview and sign-off on relevant study documents and data management and programming deliverablesPrepare mockup tables, figures and listingsDetermine analysis and data presentations specificationsProvide verification reviews on final tables, figures and listingsPerform analysis, interpret study results, and collaborate with study team to produce safety monitoring reports, interim and final reports, and publicationsRepresent the biostatistics function on project teams and in cross-functional meetings

Desired for the role:

    PhD in Statistics or a related field, with 3+ years of relevant experience. Title will be commensurate with experience.Oncology and/or Pulmonary background a plusExperience in the support of clinical studies in a pharmaceutical or biotech industry settingUnderstanding of statistical experimental design and analysis, clinical trial requirementsUnderstanding of regulatory guidelines that affect statistical deliverablesExcellent organizational and analytical skillsExcellent communication skills, both written and verbalFlexible team player with ability to balance multiple projects and instructions often with competing deadlinesCreative self-starter with strong organizational, prioritization and interpersonal skills

 

 

 


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Job Source: Ziprecruiter (Will expire by: 2021-01-04 00:00:00)

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