Smith Hanley Opprtunities

Responsible for statistical aspects of pre-clinical through Phase IV clinical trials, including experimental design, protocol development, statistical analyses, writing statistical contributions to clinical reports and collaborating with clinical investigators, physicians and medical writers. Serve as a consulting statistician for various teams, play a key role in preparing research reports and NDA submissions for various drugs. Many therapeutic areas, including CNS, GI, Oncology, Cardio, Respiratory and HIV/AIDS

Biostatistician:

Positions range from junior to senior levels. Responsible for statistical aspects of pre-clinical through Phase IV clinical trials, including experimental design, protocol development, statistical analyses, writing statistical contributions to clinical reports and collaborating with clinical investigators, physicians and medical writers. Serve as a consulting statistician for various teams, play a key role in preparing research reports and NDA submissions for various drugs. Many therapeutic areas, including CNS, GI, Oncology, Cardio, Respiratory and HIV/AIDS.

SAS Programmer:

Positions range from junior to senior levels. Responsible for editing and validating programs using SAS macros to generate listings and tables for the study reports and NDA submissions, data step manipulations for data quality assurance/validation of table, listing and summaries, using SAS to analyze clinical data from CRF's creating SAS data sets for the purpose of analysis and report writing for clinical trials (Pre-clinical through Phases IV), generating efficacy and safety reports, creating datasets and generating reports using PROC Tab, PROC Report, Data Null, SAS arrays, PROC SQL and Macros, and verify and document programs.

Clinical Data Manager:

Positions range from data coordinators to senior clinical data managers. Bachelor's Degree, with pharmaceutical experience a plus. Knowledge of structure of clinical trials databases. Database set-up, protocol review, and CRF design experience preferred. Strong communication and analytical skills required. SAS and/or Oracle experience a plus.

Oracle Clinical Programmer:

Provide programming support for some or all of the following activities: creation and maintenance of programs used for data entry, data management, data validation, statistical report generation, and program validation. Experience/Education required: Computer Programming working with Clinical Trials Data. Must have at least 2 years of programming experience and preferable 1-year clinical experience. Must have database mgt - SAS or Pl/SQL programming experience *Software preference: Oracle Clinical

Web Site: www.shcgpharm.com
Contact: ndiaz@smithhanley.com

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