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Biostatistician and Research Compliance Specialist

2 months ago

Santa Fe, New Mexico, United States Christus Health Full time
Job Summary

The Biostatistician and Research Regulatory Specialist will play a dual role in our Research department at Christus Health. This individual will provide biostatistical expertise to support the design, analysis, and interpretation of data for research, quality improvement, and performance improvement projects. They will also ensure that these projects, as well as clinical trials taking place within the department, comply with regulatory requirements and guidelines.

Key Responsibilities
  • Provide biostatistical expertise to support research projects, including data analysis and interpretation.
  • Ensure compliance with regulatory requirements and guidelines for clinical trials and research projects.
  • Collaborate with research teams to design and implement studies.
  • Develop and maintain databases and spreadsheets to support research projects.
  • Communicate research findings and results to stakeholders.
Requirements
  • Education: Bachelor's degree in biostatistics, statistics, epidemiology, public health, or a related field.
  • Certification/Licenses: Certificate of training in Good Clinical Practice must be completed within 1 month of hire.
  • Skills:
    • Proficient in programming and application of common statistical methods in medical and clinical research, such as SAS, STATA, R, or another commonly accepted analytical programming language.
    • Proficiency in using computer databases, spreadsheets, and word processing software, and electronic health systems used in research environments, or have a willingness to learn and demonstrate proficiency within six months of hire.
    • Excellent oral and written communication skills.
    • Excellent organizational skills and some knowledge of federal legislation regarding human subject research and the provision of healthcare.
    • Proficient in organizing and examining data.
    • Ability to produce clear and concise products.
    • Thorough in gathering and reporting information.
    • Flexible and able to relate well with a variety of people.
  • Experience: Three years of experience in performance improvement, clinical research, public health, or a healthcare-related field required.
Working Conditions

The Biostatistician and Research Regulatory Specialist will work in a general office environment with frequent contact with patients and VDT exposure. Long periods of sitting may be required, and keyboard usage with sound ergonomic principles is necessary. The individual must be flexible in their work schedule and willing to travel between research sites.