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Clinicaltrials Gov Jobs (NOW HIRING)

Black Canyon Consulting

Results Analyst

Bethesda, MD · On-site

Information regarding the ClinicalTrials.gov database and reporting requirements can be found at . Duties & Responsibilities: Job Responsibilities * Perform quality assurance/quality control (QA/QC) ...

Black Canyon Consulting

Results Analyst

Bethesda, MD · On-site

Information regarding the ClinicalTrials.gov database and reporting requirements can be found at . Duties & Responsibilities: Job Responsibilities * Perform quality assurance/quality control (QA/QC) ...

PSRTEK

Clinical Data Analyst-REMOTE

New York, NY · On-site

Analyze external sources (e.g., ClinicalTrials.gov) to identify inclusion/exclusion criteria and gaps in IMO content. * Prioritize clinical trials and assess opportunities for content expansion (e.g ...

Mindlance

Clinical Research Assocoate

San Diego, CA

Provide updates on study/site status as needed to ensure timely study entry and updates are reflected on ClinicalTrials.gov or equivalent * Perform periodic data reviews as requested by Study Lead

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How much do clinicaltrials gov jobs pay per hour?

As of Jun 15, 2026, the average hourly pay for clinicaltrials gov in the United States is $53.97, according to ZipRecruiter salary data. Most workers in this role earn between $37.74 and $67.31 per hour, depending on experience, location, and employer.

Does ClinicalTrials.gov pay?

ClinicalTrials.gov is a public database that provides information about clinical studies; it does not offer jobs or pay. If you are interested in working in clinical research, roles such as research coordinators or data analysts are typically paid positions within healthcare or research organizations, not directly through the database itself.

What are the main responsibilities of professionals working with ClinicalTrials.gov in a clinical research setting?

As a ClinicalTrials.gov Specialist, your primary responsibilities include registering new clinical studies, ensuring records are updated according to regulatory requirements, and submitting results within mandated timelines. You will routinely collaborate with research coordinators, investigators, and regulatory teams to gather accurate protocol information and address any questions from regulatory bodies. Attention to compliance and detail is critical, as inaccuracies can delay trial approvals or lead to penalties. You may also provide training and support to research staff regarding best practices for trial registration and reporting.

What is a Clinicaltrials Gov job?

A ClinicalTrials.gov job typically involves managing and maintaining clinical trial records on the ClinicalTrials.gov database. Responsibilities may include registering studies, updating trial information, ensuring regulatory compliance, and coordinating with research teams. Professionals in this role often work in clinical research organizations, pharmaceutical companies, or academic institutions to ensure accurate and timely reporting of trial data.

Which clinical trials pay the most money?

Clinical trial professionals such as clinical research managers, project managers, and senior coordinators tend to earn higher salaries, especially in roles requiring advanced certifications or extensive experience. Compensation can also vary based on the complexity of the trial, location, and the sponsor, with industry professionals in pharmaceutical or biotech companies generally earning more than those in academic settings.

How much does a clinical trial assistant earn?

A clinical trial assistant typically earns between $40,000 and $60,000 annually, depending on experience, location, and the organization. Entry-level positions may start lower, while experienced assistants with certifications can earn higher salaries. The role often requires familiarity with clinical trial protocols and data management tools.

What are the key skills and qualifications needed to thrive in the Clinicaltrials Gov position, and why are they important?

To excel in a ClinicalTrials.gov Specialist or Clinical Trials Regulatory Coordinator role, you need a strong understanding of clinical research, regulatory compliance, and medical terminology, usually supported by a degree in life sciences or related field. Familiarity with ClinicalTrials.gov submission protocols, electronic data capture (EDC) systems, and regulatory management software is essential. Attention to detail, strong organizational skills, and effective communication are critical soft skills for success. These capabilities ensure accurate trial registration, timely updates, and adherence to regulatory standards, supporting the integrity of clinical research operations.

How much do clinical trials pay you?

Clinical trial participants can be compensated from a few hundred to several thousand dollars, depending on the study's duration, complexity, and risk level. Compensation is typically provided as a stipend or gift card and varies by trial and location. Participants should review the specific trial details to understand the payment structure.
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Clinicaltrials Gov jobs near you
Infographic showing various Clinicaltrials Gov job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 50% In-person, and 50% Remote job distribution, with an average salary of $112,261 per year, or $54 per hour.

Registration Reviewer

Black Canyon Consulting LLC

Bethesda, MD • On-site

Other

Medical, Dental, Vision, Retirement, PTO

Posted 10 days ago

Job description

Overview
Black Canyon Consulting (BCC) is searching for a Clinical Trials Data Quality Analyst to support the ClinicalTrials.gov. 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:
Job Responsibilities
  • Perform quality assurance/quality control (QA/QC) reviews of clinical trial registration submissions for consistency with review criteria
  • Gain and use a working knowledge of the ClinicalTrials.gov Protocol Data Element Definitions (https://clinicaltrials.gov/policy/protocol-definitions) and ClinicalTrials.gov registration review criteria (https://clinicaltrials.gov/submit-studies/prs-help/protocol-registration-quality-control-review-criteria)
  • Clearly communicate (via email and record reviews) with "responsible parties" (e.g., clinical trial sponsors, designated principal investigators) regarding the consistency of clinical trial records with review criteria
  • Perform general proofreading
  • Create new documentation to help responsible parties submit their clinical trial records in accordance with established review criteria
  • Post records in accordance with established deadlines
  • Monitor data for trends or patterns of problems (e.g., consistent series of errors from a single data provider) and participate in process improvement efforts
  • Support database management activities
  • Serve as a 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
Required skills and experience
  • Bachelor's degree from an accredited college in a biomedical science, public health, or related discipline with at least 2 years of professional experience
  • Or a master's degree in a comparable field with no professional experience
  • Ability to work within a team environment and contribute to consensus-based decision making
  • 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 reside in and be authorized to work in the United States; candidates in the DMV area preferred
    • All work must be performed within the United States
Preferred Qualifications
  • Ability to identify and communicate data processing errors and content discrepancies or inconsistencies
  • Ability to identify, analyze, and solve problems creatively and independently
  • Experience in data management and quality assurance
  • General knowledge in the conduct and reporting of clinical trials
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 $65,000 - $70,000.
If you enjoy being part of a high-performing, professional, technology-focused organization, please apply today!

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