User:Genentech/BlogEntry: 2008 October 15 14:34:06 EDT

From sasCommunity

For more than 30 years, Genentech has been at the forefront of the biotechnology industry, using human genetic information to develop novel medicines for serious and life-threatening diseases. Today, Genentech is among the world’s leading biotech companies, with multiple therapies on the market for cancer and other serious medical conditions. Please take this opportunity to learn about Genentech, where we believe that our employees are our most important asset.

The following opportunity exists in our South San Francisco, CA, headquarters:

Senior Clinical Programmer Analyst

Responsibilities: The Senior Clinical Programmer Analyst (CPA) applies advanced level programming techniques and leadership to the design, development, implementation and maintenance of software in support of monitoring, reporting and analysis of clinical trial data quality. The position uses creativity and ingenuity to solve complex problems (e.g. creates reusable code, develops project/department standard code, designs interconnected programs). He/she works closely with clinical research professionals to identify project/study level needs (e.g. deliverables schedule, report approval process, standard reporting styles, etc.) and to create reports needed to identify/resolve data issues. The Senior CPA is accountable for quality and timeliness of project deliverables, as well as their suitability to the intended task. The incumbent analyzes data. The Senior CPA communicates effectively in coordinating problem resolution efforts with implementation team customers and functional peers. The position contributes continuing process, business and technical enhancements and mentors junior staff when necessary.

Requirements: The position requires a minimum of five years of SAS programming experience with a Bachelor’s degree or higher in Statistics, Math, Computer Science or equivalent experience. The candidate must have advanced skills in SAS programming language, especially data step programming and report writing. Knowledge of SAS/Graph, SAS/IntrNet and scripting languages is a plus. He/she must have an understanding of programming standards and accepted software development techniques. The applicant must have a familiarity with database theory, specifically relational database concepts and systems (e.g. ORACLE CLINICAL or Medidata Rave). He/she must have good interpersonal, verbal and written communication skills. Experience with desktop tools is required. The applicant must show the ability to work on multiple tasks simultaneously and meet project deadlines. The applicant must show the demonstrated ability to interact confidently with members of other functional areas in clinical teams. An understanding of regulatory guidelines that affect clinical deliverables is required. The candidate must have experience using SAS to process, report and analyze clinical trial data. A thorough understanding of the drug approval process is required. The candidate must have experience interacting with others for defining and implementing user defined reports. Experience in working in teams and communicating one-on-one and with groups is required. The applicant must have extensive experience in the support of at least one phase of drug development. Participation in a regulatory filing would be a plus. Experience with UNIX or similar operating system is a must.

Genentech is dedicated to fostering an environment that is inclusive and encourages diversity of thought, style, skills and perspective. To learn more about our current opportunities, please visit: http://careers.gene.com. For immediate consideration, please email: getty.jennifer@gene.com. Genentech is an Equal Opportunity Employer.