hirly

Black Canyon Consulting

Results Analyst

Bethesda, Maryland

See how you match this job — and similar ones. Free.

Upload your resume and hirly scores it against this role at Black Canyon Consulting first, then against similar open jobs, and shows where you fit and why.

PDF or DOCX, up to 12MB. No sign-up to see your matches.

Get past the screening software and onto a recruiter's desk

hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.

  • Keywords matched to this posting
  • Fit score before you apply
  • Cover letter included

Matched against 2.3M live jobs from 200,000+ employers in 200+ countries.

Tailor my resume for this job →

hirly's read of this role

Seniority
Mid level
Country
US
Work mode
On-site / unstated
First seen by hirly
30 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

Overview

Black Canyon Consulting (BCC) is searching for a Clinical Trials Data Quality Analyst to support the ClinicalTrials.gov program. Operated by the National Library of Medicine (NLM), a component of the National Institutes of Health (NIH), ClinicalTrials.gov is a registry and results database of publicly and privately supported clinical research conducted in the United States and around the world. Both registration and results submission are accomplished through the web-based Protocol Registration and Results System (PRS). Responsible parties commonly register trials and submit results prior to a journal publication. Unlike journal articles that are reviewed by both scientific colleagues and editors, data submitted to ClinicalTrials.gov are not peer-reviewed prior to posting, however specific review criteria must be met.

The successful candidate for this position will be responsible for reviewing results data submissions to ascertain whether they meet minimal review criteria for posting on ClinicalTrials.gov. Information regarding the ClinicalTrials.gov database and reporting requirements can be found at https://clinicaltrials.gov/policy/fdaaa-801-final-rule .

Duties & Responsibilities:

Perform quality assurance/quality control (QA/QC) reviews of clinical trial results submissions for consistency with review criteria

Clearly communicate (via record reviews, teleconferences, emails, workshops, etc.) with “responsible parties” (e.g., clinical trial sponsors, principal investigators, statisticians) to facilitate understanding of and adherence to submission requirements

Gain and use a working knowledge of the ClinicalTrials.gov Basic Results Data Element Definitions ( https://clinicaltrials.gov/policy/results-definitions ) and ClinicalTrials.gov results review criteria ( https://clinicaltrials.gov/submit-studies/prs-help/results-quality-control-review-criteria )

Create new documentation to help responsible parties submit their clinical trial results records in accordance with established review criteria

Devise and help implement strategies to improve the quality of submissions

Support database management activities

Serve as liaison between data providers (e.g., NIH, industry, universities, and other organizations) and ClinicalTrials.gov

Participate in weekly team meetings with NLM staff to discuss process improvement

Basic 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

Preferred Skills/Experience

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 (via coursework and/or job duties) working with and interpreting the following concepts:

Mean, median, least square mean, standard deviation, range, inter-quartile range, confidence intervals, etc.

Frequency, incidence, proportion, percentage, rate, etc.

Time-to-event measures

Parametric and non-parametric statistical tests, interpretation of p-value

Professional Skills

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

Clearance and Location Requirements

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); this is an on-site position

Must be authorized to work in the United States

Benefits and Salary

We attract the best people in the business with our competitive benefits package, including medical, dental, and vision coverage; a 401(k) plan with employer contribution; paid holidays, vacation, and tuition reimbursement.

We offer a competitive salary commensurate with experience and location. The targeted range for this position is $87,000 - $91,000.

If you enjoy being part of a high-performing, professional, technology-focused organization, please apply today!

Original posting on Black Canyon Consulting's site ↗

Want this one?

Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.

Tailor my resume for this job