Senior SAS Programmer Penumbra, Inc.
ALAMEDA, CACLINICAL AFFAIRSFULL-TIME
APPLY FOR THIS JOB
Providing critical support for Penumbra?s clinical trials, you will prepare SAS programs to enable the preparation and statistical analysis of clinical data. You will partner with other programmers, biostatisticians, and clinical data managers in the collection, analysis, and reporting of clinical data for trials.
Develop algorithms and programs to create datasets.
Produce and verify data listings, summary tables and graphs using SAS software
Import and export SAS data.
Assist data management group in performing data edit checks to facilitate data cleaning.
Maintain complete and in-depth understanding of all Clinical Data Interchange Standards Consortium (CDISC) guidance documents and implementation guides, as well as FDA guidance and regulations regarding electronic submission of data.
Keep abreast of industry trends in data mapping, data management, standards compliance methodologies, metadata management and data warehousing
Demonstrate extensive understanding of Clinical Data Acquisition Standards Harmonization (CDASH) and Study Data Tabulation Model (SDTM) standards and concepts.
Write specifications for SDTM and analysis datasets.
Manage the data warehouse used to manage libraries of clinical study data.
Interact with Regulatory Affairs, Quality Assurance, and external clinical system vendors.
Act as the subject matter expert on CDISC and good statistical programming practices.
Build efficient SAS coding or macro libraries.
WHAT YOU BRING
The desire to take on complex challenges and work with a great team.
Bachelor?s degree in Statistics, Computer Science, or a similar quantitative field.
Three to five years experience in clinical statistical programming within medical device or a related industry, such as biotechnology or pharmaceuticals.
Familiarity with Base SAS, SAS/GRAPH, SAS/ODS, and SAS/STAT. SAS Certified Base and/or Advance Programmer experience preferred.
Experience with macro programming and SAS/SQL a plus.
Excellent oral, written, and interpersonal communication skills.
Attention to detail and the ability to handle multiple tasks.
Knowledge of international regulations and clinical data standards, including CDASH, SDTM, ADaM, SHARE, BRIDG, ODM, Experience with metadata repository in clinical data a plus.
Knowledge of clinical data management systems, e.g., Oracle InForm and/or RAVE.
Expertise at using SAS in data import, data manipulation, data export, and data analysis.
WHAT WE OFFER
A collaborative teamwork environment where learning is constant and performance is rewarded.
The opportunity to be at the forefront of technology that is revolutionizing the treatment of some of the world's most devastating diseases.
A generous benefits package that includes medical, dental, vision, and life insurance; a 401(k) match; and an Employee Stock Purchase Plan. A
Penumbra, Inc. is a global leader in the development of market-shaping products to treat both neurovascular and peripheral diseases. We deliver medical devices that solve unmet clinical needs and improve patient outcomes. Founded in 2004, Penumbra?s global headquarters is located in Alameda, California with sales operations in the United States, Europe, Asia and Australia.
||Alameda, CA |