Overview Black Canyon Consulting (BCC) is seeking a Senior Technical Communications and Content Specialist to support the ClinicalTrials.gov program at the National Center for Biotechnology ...
Overview Black Canyon Consulting (BCC) is seeking a Senior Technical Communications and Content Specialist to support the ClinicalTrials.gov program at the National Center for Biotechnology ...
Overview Black Canyon Consulting (BCC) is seeking a Senior Technical Communications and Content Specialist to support the ClinicalTrials.gov program at the National Center for Biotechnology ...
Overview Black Canyon Consulting (BCC) is seeking a Senior Technical Communications and Content Specialist to support the ClinicalTrials.gov program at the National Center for Biotechnology ...
Project Data Scientist (Grant Funded, Time Limited)
Hempstead, NY · On-site
$66K - $68K/yr
Develops and maintains data pipelines to ingest, clean, and integrate data from FDA databases, ClinicalTrials.gov, and internal research datasets. * Transforms structured and semi-structured ...
Project Data Scientist (Grant Funded, Time Limited)
Hempstead, NY · On-site
$66K - $68K/yr
Develops and maintains data pipelines to ingest, clean, and integrate data from FDA databases, ClinicalTrials.gov, and internal research datasets. * Transforms structured and semi-structured ...
Clinical Trial Transparency Senior Associate
$36.50 - $50/hr
Assigns tasks, initiates workflows, follows up on all action required, and escalates alerts when needed in order to maintain content that has been made public (e.g. clinicaltrials.gov). Shares ...
Clinical Trial Transparency Senior Associate
$36.50 - $50/hr
Assigns tasks, initiates workflows, follows up on all action required, and escalates alerts when needed in order to maintain content that has been made public (e.g. clinicaltrials.gov). Shares ...
Person will be responsible for coordinating the posting of registration and disclosures on clinicaltrials.gov, EudraCT and other registries for company-wide studies. This comprises supervision of the ...
Person will be responsible for coordinating the posting of registration and disclosures on clinicaltrials.gov, EudraCT and other registries for company-wide studies. This comprises supervision of the ...
Clinical Trial Associate
$35.50 - $48.50/hr
Person will be responsible for coordinating the posting of registration and disclosures on clinicaltrials.gov, EudraCT and other registries for company-wide studies. This comprises supervision of the ...
Clinical Trial Associate
$35.50 - $48.50/hr
Person will be responsible for coordinating the posting of registration and disclosures on clinicaltrials.gov, EudraCT and other registries for company-wide studies. This comprises supervision of the ...
Person will be responsible for coordinating the posting of registration and disclosures on clinicaltrials.gov, EudraCT and other registries for company-wide studies. This comprises supervision of the ...
Person will be responsible for coordinating the posting of registration and disclosures on clinicaltrials.gov, EudraCT and other registries for company-wide studies. This comprises supervision of the ...
Sr. Clinical Trials Transparency & Disclosure Specialist
New Haven, CT · On-site
$87K - $114K/yr
Ensure timely and accurate registration, maintenance, and updating of clinical trial records in public registries, including ClinicalTrials.gov, CTIS, and other applicable regional registries.
Sr. Clinical Trials Transparency & Disclosure Specialist
New Haven, CT · On-site
$87K - $114K/yr
Ensure timely and accurate registration, maintenance, and updating of clinical trial records in public registries, including ClinicalTrials.gov, CTIS, and other applicable regional registries.
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 ...
Quick apply
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 ...
Clinical Trial Manager
Frederick, MD · On-site
$125K - $143K/yr
Ensure ClinicalTrials.gov registration and reporting requirements are met. * Monitor study metrics and status reports. * Coordinate interactions among sites, CROs, sponsors, and regulatory personnel.
Quick apply
Clinical Trial Manager
Frederick, MD · On-site
$125K - $143K/yr
Ensure ClinicalTrials.gov registration and reporting requirements are met. * Monitor study metrics and status reports. * Coordinate interactions among sites, CROs, sponsors, and regulatory personnel.
Clinical Trial Manager
$125K - $143K/yr
Ensure ClinicalTrials.gov registration and reporting requirements are met. * Monitor study metrics and status reports. * Coordinate interactions among sites, CROs, sponsors, and regulatory personnel.
Clinical Trial Manager
$125K - $143K/yr
Ensure ClinicalTrials.gov registration and reporting requirements are met. * Monitor study metrics and status reports. * Coordinate interactions among sites, CROs, sponsors, and regulatory personnel.
Maintains accurate study registration (Clinicaltrials.gov, etc.). Maintains accurate study registration (Clinicaltrials.gov, etc.). * Research Operations - Administration 10% * Provides direction to ...
Maintains accurate study registration (Clinicaltrials.gov, etc.). Maintains accurate study registration (Clinicaltrials.gov, etc.). * Research Operations - Administration 10% * Provides direction to ...
Maintains accurate study registration (Clinicaltrials.gov, etc.). Maintains accurate study registration (Clinicaltrials.gov, etc.). * Research Operations - Administration 10% * Provides direction to ...
New
Maintains accurate study registration (Clinicaltrials.gov, etc.). Maintains accurate study registration (Clinicaltrials.gov, etc.). * Research Operations - Administration 10% * Provides direction to ...
New
... projects on ClinicalTrials.gov, and prepares and submits IND or IDE applications to the FDA for BayCare-sponsored projects as required. * Required skills includes extensive knowledge of FDA ...
... projects on ClinicalTrials.gov, and prepares and submits IND or IDE applications to the FDA for BayCare-sponsored projects as required. * Required skills includes extensive knowledge of FDA ...
Director / Senior Director of Regulatory Affairs
New York, NY · On-site
$220K - $300K/yr
Oversee ClinicalTrials.gov listings and ensure all regulatory commitments and timelines are tracked and met. Submission Operations Oversee eCTD publishing and submission infrastructure, managing ...
Director / Senior Director of Regulatory Affairs
New York, NY · On-site
$220K - $300K/yr
Oversee ClinicalTrials.gov listings and ensure all regulatory commitments and timelines are tracked and met. Submission Operations Oversee eCTD publishing and submission infrastructure, managing ...
Other duties include reporting and registering clinical trials to the NCI's Clinical Trial reporting Program (CTRP) for accrual information and the clinicaltrials.gov registry for study outcome ...
Other duties include reporting and registering clinical trials to the NCI's Clinical Trial reporting Program (CTRP) for accrual information and the clinicaltrials.gov registry for study outcome ...
Regulatory Operations Assistant - I
Foster City, CA · On-site +1
... ClinicalTrials.gov and the EU Clinical Trial Register. Disclosures is also responsible for the EMA Policy 0070 (Publication of Clinical Data and Reports) activities. PROJECT INVOLVEMENT: Does not ...
Regulatory Operations Assistant - I
Foster City, CA · On-site +1
... ClinicalTrials.gov and the EU Clinical Trial Register. Disclosures is also responsible for the EMA Policy 0070 (Publication of Clinical Data and Reports) activities. PROJECT INVOLVEMENT: Does not ...
... ClinicalTrials.gov. Coordinate project
... ClinicalTrials.gov. Coordinate project
Assistant Director, Operations
Bronx, NY · On-site
$120K/yr
Oversees compliance with ClinicalTrials.gov, including an understanding of intersecting regulations governing human subjects research. * Serves a key leader within the institution, proactively ...
Assistant Director, Operations
Bronx, NY · On-site
$120K/yr
Oversees compliance with ClinicalTrials.gov, including an understanding of intersecting regulations governing human subjects research. * Serves a key leader within the institution, proactively ...
Familiarity with PubMed, ClinicalTrials.gov, and other sources of clinical and scientific content * Experience in publication writing, including primary manuscripts, reviews, abstracts and poster ...
Quick apply
Familiarity with PubMed, ClinicalTrials.gov, and other sources of clinical and scientific content * Experience in publication writing, including primary manuscripts, reviews, abstracts and poster ...
Clinicaltrials Gov information
See salary details
$12.50 - $19.71
5% of jobs
$19.71 - $26.92
7% of jobs
$26.92 - $34.13
7% of jobs
$36.99 is the 25th percentile. Wages below this are outliers.
$34.13 - $41.35
13% of jobs
$41.35 - $48.56
9% of jobs
The median wage is $53.06 / hr.
$48.56 - $55.77
13% of jobs
$55.77 - $62.98
17% of jobs
$64.93 is the 75th percentile. Wages above this are outliers.
$62.98 - $70.19
13% of jobs
$70.19 - $77.40
9% of jobs
$77.40 - $84.62
4% of jobs
$84.62 - $91.83
2% of jobs
$12
$53
$91
How much do clinicaltrials gov jobs pay per hour?
As of Aug 4, 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.
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Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 27 days ago
Job description
Overview
Black Canyon Consulting (BCC) is seeking a Senior Technical Communications and Content Specialist to support the ClinicalTrials.gov program at the National Center for Biotechnology Information (NCBI), part of the National Institutes of Health (NIH).
This role is ideal for a versatile communications professional who combines strong technical writing and editing skills with the ability to coordinate across multiple teams, manage content review workflows, and ensure consistency across a wide range of communication products. The successful candidate will help develop and maintain high-quality content that supports ClinicalTrials.gov users, program operations, and regulatory requirements.
Duties & Responsibilities:
Job Responsibilities
Preferred Qualifications
Writing and editing samples may be requested during the interview process.
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. If you enjoy being part of a high-performing, professional, technology-focused organization, please apply today!
Black Canyon Consulting (BCC) is seeking a Senior Technical Communications and Content Specialist to support the ClinicalTrials.gov program at the National Center for Biotechnology Information (NCBI), part of the National Institutes of Health (NIH).
This role is ideal for a versatile communications professional who combines strong technical writing and editing skills with the ability to coordinate across multiple teams, manage content review workflows, and ensure consistency across a wide range of communication products. The successful candidate will help develop and maintain high-quality content that supports ClinicalTrials.gov users, program operations, and regulatory requirements.
Duties & Responsibilities:
Job Responsibilities
- Develop, edit, and maintain website content, user guides, FAQs, training materials, policies, and other program documentation.
- Review content for clarity, accuracy, consistency, usability, and alignment with plain language principles.
- Ensure consistency in messaging, terminology, style, and formatting across multiple content channels and products.
- Translate complex technical, scientific, and regulatory information into clear, audience-appropriate communications.
- Coordinate content reviews and approvals among subject matter experts, technical teams, customer support staff, and leadership.
- Create and manage Jira tickets and track content-related action items to support publication and review workflows.
- Contribute to style guides, editorial standards, templates, and content governance processes.
- Develop and maintain a content maintenance plan and review schedule to help ensure website content, documentation, training materials, and related resources remain accurate, current, and aligned with program needs.
- Maintain documentation of content review processes, editorial workflows, governance practices, and content standards used across teams to promote consistency, transparency, and efficient content management.
- Collaborate with software developers and program stakeholders to ensure documentation accurately reflects system functionality, policies, and program requirements.
- Identify opportunities to improve content quality, user experience, and communication effectiveness.
- Bachelor's degree in Communications, Technical Writing, English, Journalism, Public Health, Information Science, Computer Science, or a related field (or equivalent experience).
- Experience developing and editing technical documentation, web content, instructional materials, or other complex written products.
- Exceptional technical writing, copyediting, and proofreading skills.
- Ability to translate complex concepts into clear, concise, user-focused content.
- Experience coordinating reviews and collaborating with multiple stakeholders.
- Strong organizational and project coordination skills.
- Ability to work independently, manage competing priorities, and proactively drive assignments to completion.
- Excellent written and verbal communication skills.
Preferred Qualifications
- Local candidate preferred who is able to work in a collaborative hybrid environment
- Experience supporting federal, scientific, healthcare, clinical research, or regulated programs.
- Familiarity with ClinicalTrials.gov, PRS, clinical research, or biomedical information systems.
- Knowledge of content governance, style guide development, and editorial workflows.
- Familiarity with FDAAA 801, NIH clinical trial policies, or similar regulatory frameworks.
- Experience with Jira, Confluence, SharePoint, Microsoft 365, Adobe Acrobat, Google Analytics, Qualtrics, or similar tools.
- Experience with plain language writing and digital content best practices.
Writing and editing samples may be requested during the interview process.
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. If you enjoy being part of a high-performing, professional, technology-focused organization, please apply today!