Clinical Research Management - San Antonio, TX

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Growing and well-respected biomedical (clinical, basic and applied) research firm has openings at Lackland AFB . If you are passionate about research, and are looking for a firm that shares your passion, and provides competitive salaries with a strong benefits package, join the ClinicalRM team.

We are currently seeking a Biostatistician for the San Antonio, Texas area.

Develops strategies using statistical analysis to draw scientific conclusions or predications based on data summaries or statistical analysis. Determines which statistical methodology to apply based on comprehensive knowledge of parametric and nonparametric hypothesis tests, univariate and multivariate linear and nonlinear modeling, life table analysis, time series analysis and instrument validation procedures. Detailed support shall include, at a minimum:

Development of detailed data and process models.

Indepth knowledge and profieciency to delineate requirements within Statistical Package for the Social Sciences (SPSS) and Statistical Analysis Software (SAS).

Provide biostatistical consultation to PIs or colleagues. Coordinate database preparation for data analysis, including assessment for any data transformation requirements.

Written detailed analysis plans and descriptions of analyses and findings for research protocols or reports.

Indepth analysis of clinical or survey data using statistical approaches including but not limited to longitudinal analysis, mixed effect modeling, logistic regression analysis and model building techniques.

Reviews clinical or medical research protocols and recommends and conducts appropriate statistical analyses.

Prepare statistical data for inclusion in data monitoring committees, AF/DoD/Federal regulatory agencies, managers or investigators.

Calculate samples size requirements for clinical studies.

Determines project plans, timelines, or technical objectives for statistical aspects of biological research studies.

Translates statistical information into documents relevant to manuscripts/ presentation being published by investigators. Prepares written synthesis of analysis results for inclusion in research manuscripts, presentations, and reports. Assesses the adequacy of the presentation of data, methods and purported objectives of the research projects.

Master of Science required with a minimum of 8 years of experience in the field of bio-medical and laboratory management within the last 9 years required with experience related to conducting clinical research and analyzing medical data.

Must be able to work independently following a brief period of specific technical training.

Qualified candidates will receive consideration for employment without regard to race, color, religion, sex, or national origin. Candidates for positions under ClinicalRM’s contracts with the Department of Defense (DoD) will be required to pass one or more background/security investigations conducted by the DoD, U.S. Army, or other Federal Government agency. Such investigations may include criminal records and credit history checks.

ClinicalRM is an Affirmative Action-Equal Opportunity Employer

“NorthCoast 99” Best Places to Work recipient