Prepare Clinical Studies Reports - 80%: Review clinical study files and databases to complete study dates, demographics etc. Review protocols to determine methodologies used in study. Review data in statistical analysis files against source data. Conduct basic statistical analyses of clinical data and incorporate into report statistical description and results. Adjust standard templates to meet individual study requirements. Identify documentation inconsistencies and deficiencies to be addressed by study staff. Ensure reports adhere to standards for quality, format and style. Peer-Review of Reports - 20%: Review reports written by other preparers for accuracy and completeness. $112,611/year. Required: Bachelor’s degree in Computer Science, Mathematics or related/equivalent plus 3 years experience in Pharma Industry, Clinical Data Manager, Research Technician, Regulatory Specialist, Clinical Research, Data Analyst or related. Must have 3 years experience (simultaneous/concurrent with above 3 years experience) with scientific Excel computing; Qlikview or Tibco Spotfire; programming with large datasets and developing programs, testing and documentation. Resumes to resumes@irionline.com. May telecommute from any location in the US.