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Remote Seafood Quality Control Jobs (NOW HIRING)

Corvel

Clinical Review QC Auditor

Fort Worth, TX · Remote

$68.57K - $104.84K/yr

CERIS in Fort Worth, TX is seeking a DRG Quality Control/Clinical Auditor. The Diagnostic Related ... This is a remote position. ESSENTIAL FUNCTIONS & RESPONSIBILITIES: * Review medical records to ...

Corvel

Clinical Review QC Auditor

$68.57K - $104.84K/yr

CERIS in Fort Worth, TX is seeking a DRG Quality Control/Clinical Auditor. The Diagnostic Related ... This is a remote position. ESSENTIAL FUNCTIONS & RESPONSIBILITIES: * Review medical records to ...

CERiS

Clinical Review QC Auditor

Fort Worth, TX · Remote

$68.57K - $104.84K/yr

CERIS in Fort Worth, TX is seeking a DRG Quality Control/Clinical Auditor. The Diagnostic Related ... This is a remote position. ESSENTIAL FUNCTIONS & RESPONSIBILITIES: * Review medical records to ...

CERiS

Clinical Review QC Auditor

Fort Worth, TX · On-site +1

$68.57K - $104.84K/yr

CERIS in Fort Worth, TX is seeking a DRG Quality Control/Clinical Auditor. The Diagnostic Related ... This is a remote position. ESSENTIAL FUNCTIONS & RESPONSIBILITIES: * Review medical records to ...

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How much do remote seafood quality control jobs pay per hour?

As of May 31, 2026, the average hourly pay for remote seafood quality control in the United States is $21.48, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $24.04 per hour, depending on experience, location, and employer.

What is the difference between Remote Seafood Quality Control vs Remote Seafood Processing Technician?

AspectRemote Seafood Quality ControlRemote Seafood Processing Technician
CertificationsFood safety, HACCP, QA certificationsFood safety, HACCP, equipment operation
Work EnvironmentOffice, home, or remote quality assurance settingsRemote monitoring of processing lines or equipment
Industry UsageQuality assurance, inspection, compliance rolesProcessing line support, equipment troubleshooting
Search IntentQuality control, inspection, food safetyProcessing, equipment, technical support

Remote Seafood Quality Control focuses on ensuring seafood products meet safety and quality standards through inspections and audits, often in a remote or office setting. In contrast, Remote Seafood Processing Technicians support processing operations remotely, focusing on equipment and technical troubleshooting. Both roles require food safety certifications but differ in daily tasks and work environment.

More about Remote Seafood Quality Control jobs
What cities are hiring for Remote Seafood Quality Control jobs? Cities with the most Remote Seafood Quality Control job openings:
What are the most commonly searched types of Seafood Quality Control jobs? The most popular types of Seafood Quality Control jobs are:
What states have the most Remote Seafood Quality Control jobs? States with the most job openings for Remote Seafood Quality Control jobs include:
What job categories do people searching Remote Seafood Quality Control jobs look for? The top searched job categories for Remote Seafood Quality Control jobs are:
Remote Seafood Quality Control jobs near you
Infographic showing various Remote Seafood Quality Control job openings in the United States as of May 2026, with employment types broken down into 2% Locum Tenens, 6% As Needed, 11% Full Time, 11% Part Time, 8% Temporary, and 62% Contract. Highlights an 13% Physical, 5% Hybrid, and 82% Remote job distribution, with an average salary of $44,668 per year, or $21.5 per hour.

Clinical QC Consultant

Medvacon Life Sciences, LLC

Wayne, NJ • Remote

Full-time

Posted 11 days ago

Job description

Clinical QC Consultant – Job Description
Position Overview
The Clinical QC Consultant is responsible for ensuring the quality, accuracy, and compliance of clinical trial documentation and data. This role supports clinical operations by performing quality control reviews and ensuring adherence to regulatory requirements and internal standards.
Key Responsibilities
  • Perform QC review of clinical documents, including:
    • Clinical study reports (CSRs)
    • Protocols and protocol amendments
    • Informed consent forms (ICFs)
    • Monitoring visit reports
    • Trial master file (TMF) documents
  • Ensure compliance with:
    • Food and Drug Administration (FDA) regulations
    • International Council for Harmonisation (ICH) guidelines
    • Good Clinical Practice (GCP) standards
  • Verify data accuracy and consistency across clinical systems (e.g., EDC, CTMS, TMF)
  • Identify discrepancies, errors, or missing information and communicate findings to clinical teams
  • Ensure proper documentation, version control, and audit readiness
  • Support inspection readiness activities and participate in internal audits
  • Collaborate with cross-functional teams including Clinical Operations, Data Management, and Regulatory Affairs
  • Assist in the preparation of protocols (including the writing of administrative letters for protocols and summary of changes for protocol amendments) and CSRs.
  • Assist in the preparation of study-level documentation required for clinical trials (e.g., CSR appendices, shell drafts)
  • Edit CSR statistical analysis plans and table/figure/listing specifications for grammar, format, and consistency.
  • Support authoring of protocols, investigator brochures, CSRs and other study-level documentation required for clinical trials.
  • Edit submission documents (sections of CSRs, IND/CTA, NDA, MAA,  requests for information and briefing documents. etc.) for regulatory agencies.
  • Reviews CSR statistical analysis plans and table/figure/listing specifications for grammar, format, and consistency.

Required Qualifications
  • Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related field
  • 5+ years of experience in clinical research, QA/QC, or clinical operations
  • Strong knowledge of FDA regulations, ICH guidelines, and GCP
  • Experience reviewing clinical trial documentation and TMF management
  • High attention to detail and strong analytical skills

Preferred Qualifications
  • Experience in hepatology or rare disease clinical trials (relevant to focus areas)
  • Prior experience in a biotech or pharmaceutical company
  • Familiarity with electronic systems such as Veeva Vault, Medidata, or similar

Key Skills
  • Quality control and audit readiness
  • Documentation review and compliance
  • Communication and collaboration
  • Problem-solving and critical thinking

Work Environment
  • Contract/consultant role
  • Remote or hybrid (depending on project needs)
  • May require collaboration across global teams

Important Notice: Protecting Your Information
Medvacon Talent Acquisition only conducts initial video interviews via Microsoft Teams or Zoom. All communication will come from an email address ending in @medvacon.com. If you receive a message that seems suspicious or is not from our official domain, please report it immediately to jobs@medvacon.com.

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