Results Analyst

The role

The Results Analyst will review clinical trial results submissions to ensure they meet minimal review criteria for ClinicalTrials.gov. This role involves performing quality assurance, communicating with responsible parties, and supporting database management.

What you will do

• Perform quality assurance/quality control (QA/QC) reviews of clinical trial results submissions
• Communicate with responsible parties to facilitate understanding of submission requirements
• Gain and use knowledge of ClinicalTrials.gov Basic Results Data Element Definitions and review criteria
• Create new documentation to help responsible parties submit clinical trial results records
• Devise and help implement strategies to improve the quality of submissions
• Support database management activities
• Serve as liaison between data providers and ClinicalTrials.gov
• Participate in weekly team meetings with NLM staff

Required qualifications

• Master’s degree in biomedical science and/or mathematics-related discipline (epidemiology, biostatistics, neuroscience, biochemistry, etc.)
• 3+ years’ experience with standard mathematical concepts and statistics (correlations, trends, significance, etc.)
• 1+ year experience with standard quantitative measures for health studies
• Ability to work within a team environment and contribute to consensus-based decision making
• Ability to identify, analyze, and solve problems creatively and independently
• Ability to handle multiple tasks simultaneously and shift priorities as directed
• Ability to work efficiently with team members in a fast-paced environment
• Excellent oral and written communication skills
• Excellent interpersonal skills and ability to work with people at every level
• General computer skills with a proficiency in MS Word, Outlook, Excel, and PowerPoint
• Must be able to obtain and maintain a Public Trust clearance
• Must be authorized to work in the United States

Nice to have

• Ph.D. in biomedical science and/or mathematics-related discipline (epidemiology, biostatistics, neuroscience, biochemistry, etc.)
• Background knowledge relevant to understanding and interpreting clinical trial data and statistics
• 1+ year experience with analysis and reporting of clinical trial data
• Strong critical thinking, analysis, and problem-solving skills
• Ability to critically appraise clinical trial design and methodology and to identify internal inconsistencies in clinical trial data reporting
• Experience working with and interpreting mean, median, least square mean, standard deviation, range, inter-quartile range, confidence intervals, etc.
• Experience working with frequency, incidence, proportion, percentage, rate, etc.
• Experience working with time-to-event measures
• Experience working with parametric and non-parametric statistical tests, interpretation of p-value

Benefits

• medical, dental, and vision coverage
• 401(k) plan with employer contribution
• paid holidays
• vacation
• tuition reimbursement

Before you apply

• Must be able to obtain and maintain a Public Trust clearance
• Must be located within 40 miles of the NIH Bethesda campus (or willing to relocate)
• Must be authorized to work in the United States

About the company

Black Canyon Consulting (BCC) is a professional, technology-focused organization.