Manager/Sr. Manager, Statistical Programming

San Francisco, CA 94158 | Contract

Post Date: 04/06/2017 Job ID: 10978

Bayside Solutions is seeking a Manager/Sr. Manager, Statistical Programming to be part of our Client’ s team in San Francisco. This is an opportunity to work with a local Biopharmaceutical company focusing on the discovery, development, and commercialization of novel therapeutics to treat serious unmet medical needs.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at

Manager/Sr. Manager, Statistical Programming

Job Benefits:

  • An opportunity to join a patient-focused organization that is driven to develop and commercialize novel drugs for treating rare diseases.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities
  • Participate in CRF design, database review, data management plan, data review, data validation procedures, and review of data listings
  • Design, develop, implement, and maintain software for the monitoring of ongoing studies, reporting, and analysis of clinical trials
  • Provide consistency across protocols within a project on CRFs, database design, analyses files, and tables, listings, and graphs
  • Produce data listings, summary tables and graphics for interim and final analyses and publications
  • Create statistical files for statistical analysis.
  • Integrate data across studies within a project.
  • Test, document, review and validate all programs according to department guidelines
  • Provide consulting and systems support for applications software. 
  • Develop new applications software and identify key feature set
  • Coordinate data transfer and/or programming standards with CROs and vendors.
  • Collaborate with other biometrics functions for all activities related to analyses of clinical trial data.
  • Responsible for execution of ad-hoc requests, manuscripts, posters, and presentations.
  • Act independently to determine methods and procedures on new assignments
  • Work with minimal supervision



Required Qualifications:

  • Minimum of 8 years of SAS programming in the pharmaceutical or biotechnology industry with a BA/BS in computer science, statistics, math or MA/MS with 8 years of experience.
  • Expertise in SAS programming language (especially data step, and summarization procedures), report generation, and standards for programming and validation
  • Experienced in macro writing. Knowledge of advanced statistical procedures in SAS including LIFETEST, MIXED, GLM, especially SAS/GRAPH
  • Experience with CDISC data standards required.
  • Knowledge of database and data warehouse theory - Data mining experience is a plus
  • Experience as a senior statistical programmer level in a pharmaceutical or CRO working in a FDA regulated environment
  • Experience with Clinical Study Reports and NDA submission.
  • Understanding of regulatory guidelines that affect statistical deliverable
  • Ability to work on multiple tasks simultaneously and meet project deadlines
  • Excellent verbal/written and interpersonal skills required for working successfully in a cross-functional team environment
  • Communicate and collaborate effectively with cross-functional teams in face-to-face conversation, by telephone, and by email


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