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Ctd Jobs (NOW HIRING)

YO AI Labs

Regulatory Affairs Expert - Remote

Dallas, TX · Remote

$50 - $80/hr

Ensure adherence to ICH guidelines and CTD/eCTD requirements. * Identify regulatory risks, inconsistencies, and unsupported claims. * Prepare structured, guideline-based written feedback. Required ...

YO AI Labs

Regulatory Affairs Expert - Remote

Austin, TX · Remote

$50 - $80/hr

Ensure adherence to ICH guidelines and CTD/eCTD requirements. * Identify regulatory risks, inconsistencies, and unsupported claims. * Prepare structured, guideline-based written feedback. Required ...

YO AI Labs

Regulatory Affairs Expert - Remote

Boston, MA · Remote

$50 - $80/hr

Ensure adherence to ICH guidelines and CTD/eCTD requirements. * Identify regulatory risks, inconsistencies, and unsupported claims. * Prepare structured, guideline-based written feedback. Required ...

YO AI Labs

Regulatory Affairs Expert - Remote

Atlanta, GA · Remote

$50 - $80/hr

Ensure adherence to ICH guidelines and CTD/eCTD requirements. * Identify regulatory risks, inconsistencies, and unsupported claims. * Prepare structured, guideline-based written feedback. Required ...

YO AI Labs

Regulatory Affairs Expert - Remote

Phoenix, AZ · Remote

$50 - $80/hr

Ensure adherence to ICH guidelines and CTD/eCTD requirements. * Identify regulatory risks, inconsistencies, and unsupported claims. * Prepare structured, guideline-based written feedback. Required ...

YO AI Labs

Regulatory Affairs Expert - Remote

Seattle, WA · Remote

$50 - $80/hr

Ensure adherence to ICH guidelines and CTD/eCTD requirements. * Identify regulatory risks, inconsistencies, and unsupported claims. * Prepare structured, guideline-based written feedback. Required ...

YO AI Labs

Regulatory Affairs Expert - Remote

Chicago, IL · Remote

$50 - $80/hr

Ensure adherence to ICH guidelines and CTD/eCTD requirements. * Identify regulatory risks, inconsistencies, and unsupported claims. * Prepare structured, guideline-based written feedback. Required ...

YO AI Labs

Regulatory Affairs Expert - Remote

Houston, TX · Remote

$50 - $80/hr

Ensure adherence to ICH guidelines and CTD/eCTD requirements. * Identify regulatory risks, inconsistencies, and unsupported claims. * Prepare structured, guideline-based written feedback. Required ...

medac Gesellschaft für klinische Spezialpräparate mbH

$90 - $120/hr

Author, review and lead high‑quality clinical and regulatory documents (CTD), including Clinical Overview & Clinical Summary, Clinical Expert Statements, Risk Management Plans (RMPs), SmPC, CCDS ...

New

US Tech Solutions

CMC Manager

Morristown, NJ · On-site

Draft or update the technical registration dossiers (CTD Module III and QOS or equivalent) of pharmaceutical products * Evaluate change requests with a goal of defining technical requirements ...

Staffingine LLC

CMC Writer

Paramus, NJ · On-site

Authors a range of clinical documents, including regulatory documents following defined templates, NDA/MAA CTD submission documents, investigator brochures, briefing documents, and responses to ...

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Ctd information

See salary details

$14

$23

$33

How much do ctd jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for ctd in the United States is $23.65, according to ZipRecruiter salary data. Most workers in this role earn between $19.71 and $26.92 per hour, depending on experience, location, and employer.

What is a CTD?

A CTD (Clinical Trial Director) is responsible for overseeing the planning, execution, and management of clinical trials in the healthcare or pharmaceutical industry. They ensure compliance with regulatory guidelines, coordinate cross-functional teams, and monitor trial progress to achieve research objectives. Their role is crucial in bringing new medical treatments and therapies to market efficiently and safely.

What are the key skills and qualifications needed to thrive as a Clinical Trial Director (CTD), and why are they important?

To thrive as a Clinical Trial Director (CTD), you need expertise in clinical research, regulatory compliance, project management, and typically an advanced degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification is highly valued. Strong leadership, attention to detail, and effective communication enable CTDs to coordinate teams and ensure protocol adherence. These capabilities are crucial for delivering successful, compliant trials that meet scientific and regulatory standards.

What are some common challenges faced by CTD (Clinical Trial Data) professionals when managing clinical trial data, and how can they be addressed?

CTD professionals often encounter challenges such as ensuring the accuracy and integrity of large datasets, meeting tight regulatory deadlines, and coordinating with cross-functional teams like clinical operations and biostatistics. Addressing these challenges requires strong attention to detail, effective communication, and proficiency with data management systems and regulatory standards. Many organizations support CTD professionals through ongoing training, robust data validation tools, and regular team meetings to address issues promptly and collaboratively.

What is the difference between Ctd vs Radiologic Technologist?

AspectCtdRadiologic Technologist
Required CredentialsCertification in Cardiothoracic Diagnostic procedures, often includes ARRT or equivalentARRT certification in Radiography, ARRT or ARDMS in specialized areas
Work EnvironmentHospitals, clinics specializing in cardiology, diagnostic labsHospitals, outpatient imaging centers, clinics
Industry UsagePrimarily in cardiology and diagnostic labsBroadly in medical imaging across various specialties

While both Ctd and Radiologic Technologists work in medical imaging environments, Ctd specialists focus on cardiothoracic diagnostics, requiring specific certifications and working mainly in cardiology settings. Radiologic Technologists have a broader scope across imaging modalities, including X-rays and MRIs, in diverse healthcare environments.

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Ctd jobs near you
Infographic showing various Ctd job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $49,183 per year, or $23.6 per hour.

Regulatory Affairs Expert - Remote

YO AI Labs

Texas City, TX • Remote

$50 - $80/hr

Full-time

Posted 10 days ago

Job description

Job Title: Regulatory Affairs Specialist
Location: Remote
Job Type: ContractJob Description

We are seeking an experienced Regulatory Affairs Specialist to support AI-driven healthcare projects by reviewing and evaluating regulatory documentation. The role involves assessing clinical documents, ensuring compliance with regulatory guidelines, identifying inconsistencies, and providing clear, evidence-based feedback to improve AI-generated regulatory content.

Key Responsibilities

  • Review and evaluate clinical and regulatory documentation.

  • Assess regulatory submissions and responses for accuracy and compliance.

  • Ensure adherence to ICH guidelines and CTD/eCTD requirements.

  • Identify regulatory risks, inconsistencies, and unsupported claims.

  • Prepare structured, guideline-based written feedback.

Required Qualifications

  • 5+ years of Regulatory Affairs experience in the pharmaceutical, biotech, or CRO industry.

  • Experience with clinical submissions, regulatory documentation, and health authority interactions.

  • Strong knowledge of ICH guidelines and CTD/eCTD structure.

  • Excellent analytical, critical thinking, and written communication skills.

  • Degree in Life Sciences, Pharmacy, Medicine, or a related field.