Senior Statistical Programmer (Permanent role)

United States full timeRemote

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senior

H1B: yes

Clinchoice Senior Statistical Programmer leads statistical programming activities for clinical trials, including programming, validation, and oversight of deliverables. The role requires collaboration with cross-functional teams and management of internal and external programming resources.

Responsibilities

Programing for clinical trials:
Program and validate derived datasets, tables, figures, listings. Process data from the external sources.
Perform ad hoc exploratory analyses for publications and programming support other functions of Research and Development or other organizations.
Oversee programing work/deliverables from CROs.
Contribute to the design/implementation/review of Case Report Form, Data Transfer Specification, Statistical Analysis Plan, SDTM/ADaM Specification documents, Define packages.
Electronic submissions:
Program and validate CDISC compliant deliveries for the electronic submissions.
Support in the creation of supporting documentation for submissions.
Project Management:
Ensure programming deliverables are on time and of high quality.
Help managing internal contractors and external vendors.
Standards and Guidelines:

Qualification

Strong knowledge of industry standards

Required

Bachelor or Master degree in Computer Science, Mathematics, Engineering, Medical or related discipline
BS with more than 5 or MS with 3 years of experience in statistical programming (SAS, R) in the pharmaceutical industry
Working knowledge of SAS and its various components
Knowledge of R programming in clinical trials
Familiarity with the drug development process
Strong SAS and SAS Macro language skills
Strong knowledge of industry standards
Ability to work on data integrations (ISS and ISE)

Company

Clinchoice

View company page

Source: greenhouse

Active within the past hour

Remote-friendly

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Must-Have Skills for This Role

SASSAS Macro languageR programmingCDISCStatistical Analysis PlanSDTM

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