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Title:Sr. Clinical Programmer Analyst Clinical Data Management
Location:CA - South San Francisco

The Senior Clinical Programmer Analyst 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.

  • Uses creativity and ingenuity to solve complex problems (e.g. creates reusable code, develops project/ department standard code, designs interconnected programs).
  • 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.
  • Analyzes data capture.
  • Communicates effectively in coordinating problem resolution efforts with implementation team customers and functional peers.
  • Contributes continuing process, business, and technical enhancements and mentors junior staff when necessary.

  • A minimum of 5 years of SAS programming with a BS or higher in statistics, math, computer science, or equivalent experience.
  • Advanced skills in SAS programming language, especially data step programming and report writing.
  • Knowledge of SAS/Graph, SAS/IntrNet, and scripting languages a plus.
  • Understanding of programming standards and accepted software development techniques.
  • Knowledge and familiarity with data base theory, specifically relational database concepts and systems e.g. ORACLE CLINICAL or Medidata Rave.
  • Good interpersonal skills.
  • Good verbal and written communication skills.
  • Experience with desktop tools.
  • Ability to work on multiple tasks simultaneously and meet project deadlines.
  • Demonstrated ability to interact confidently with members of other functional areas in clinical teams.
  • Demonstrated competence in data warehouse design and implementation, and integrated database design.
  • Understanding of regulatory guidelines that affect clinical deliverables.
  • Experience using SAS to process, report, and analyze clinical trial data.
  • Thorough understanding of the drug approval process.
  • Experience interacting with others for defining and implementing user defined reports.
  • Experience in working in teams and communicating one-on-one and with groups.
  • 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.

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