Zeno Management, Inc. seeks a Senior Manager, Statistical Programming and Reporting in San Diego, California or remote anywhere in the U.S. The Senior Manager, Statistical Programming and Reporting will utilize their experience working in a statistical programming position for pharmaceutical or biotechnology clinical research and/or development to support ongoing efficacy and safety analyses across entire clinical pipeline programs. This role will help with critical data interpretations used for internal decision-making and health authority interactions.
Specific responsibilities for the role include:
- Preparing clinical and statistical reports using SAS;
- Creating tables, listings, figures (TLFs) and analysis datasets to support medical and clinical review, and to enable the data-driven operation and decision in oncology-related clinical trials;
- As the owner of business intelligence, communicating with management and project teams for report requirements and specifications and standardize the basic reports in supporting the Risk-based Monitoring and solving operational or data problems for clinical trials;
- Working with study statisticians to support abstracts, posters, manuscripts and other oncology related clinical publications;
- Understanding Clinical Data Interchange Standards Consortium (CDISC), Study Data Tabulation Model (SDTM) and Analysis Data Model (ADaM) standards and regulatory requirements;
- Creating SDTM/ADaM datasets while following CDISC standards;
- Developing independent programs to validate analysis datasets and TLFs generated by vendors, ensuring compliance with CDISC and submission requirements;
- Working on oncology studies to perform safety and efficacy analysis; and
- Developing and maintaining SAS programming macros, templates and utilities to support internal data review, monitoring, data reporting and visualization.
Education Requirement:
Bachelor’s degree or foreign equivalent in pharmacy, statistics, or a related field.
Experience Requirement:
Five (5) years of experience working in a statistical programming position for pharmaceutical or biotechnology clinical research and/or development.
Three (3) years of experience in:
- Creating SDTM/ADaM datasets while following CDISC standards;
- Creating Tables, Data Listings, and Figures (“TLFs”);
- Developing independent programs to validate analysis datasets and TLFs generated by vendor while ensuring compliance with CDISC and submission requirements; and
- Developing and maintaining SAS programming macros to support internal data review and monitoring.
Experience must also include two (2) years of experience working on oncology-related projects.
Travel:
None. This position permits teleworking/remote working anywhere in the U.S.
Pay:
Pay is $164,000 to $180,000, depending on experience.
Employer Contact:
To apply, email resume to Sheena Delgado ([email protected]) referencing REQ 211017.
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