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Quality Assurance Research Associate Jobs (NOW HIRING)

Opportunity Type Regular Summary The Research Associate supports and leads priority research and ... Provide technical review and quality assurance for priority HFHI research, including research ...

The Research Associate 1, SOM supports research activities for the assigned division by conducting ... Perform data verification, quality assurance, and database reconciliation activities to ensure ...

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Quality Assurance Associate

Commack, NY ยท On-site

$25.50 - $29/hr

We are looking to add Quality Assurance Associates to staff!! This position is in the office Monday-Friday during normal business hours. We are looking to hire 2 Quality Assurance Associates ASAP!

New

Be Seen First

Quality Assurance Associate

Commack, NY ยท On-site

$25.50 - $29/hr

We are looking to add Quality Assurance Associates to staff!! This position is in the office Monday-Friday during normal business hours. We are looking to hire 2 Quality Assurance Associates ASAP!

New

The Research Associate 1, SOM supports research activities for the assigned division by conducting ... Perform data verification, quality assurance, and database reconciliation activities to ensure ...

Clinical Trial Quality Assurance Associate * Assist Auditors with Sponsor audits and regulatory ... We assist clinical research throughout the lifecycle of development, from drug concept to ...

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As of Sep 15, 2026, the average hourly pay for quality assurance research associate in the United States is $29.29, according to ZipRecruiter salary data. Most workers in this role earn between $18.75 and $34.38 per hour, depending on experience, location, and employer.

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Infographic showing various Quality Assurance Research Associate job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $60,925 per year, or $29.3 per hour.

Scientific Research Associate

New Haven, CT โ€ข Hybrid

VIRSCIO, INC.
Biotechnology Research and Developmentย โ€ขย 11 - 50 employees

Full-time

Re-posted 17 days ago


Job description

Job Title

Scientific Research Associate

Department

Pathology

Reports To

Director of Pathology

Job Overview

The Scientific Research Associate will work across Virscio to review study protocols, support and set up study specific electronic data capture systems (Provantis, Excel, Word), manage study scheduling, pull out and organize data to enable downstream analysis, QC draft reports, and draft SOPS and report templates. The Scientific Research Associate may work with Sponsors to achieve study-specific deliverables and timelines.

Your main stakeholders will include Pathology, Histology, Molecular, and Ophthalmology. Your collaborators will include Data Management, Quality Assurance, Study Coordinators, Study Managers, Finance, and the Veterinary Team.

Work Location

Strong preference for individuals committed to working at least 4 days a week at our facility in New Haven, CT; remote worker considered for the right candidate.ย 

Unique Working Hours Considerations

None

Type of Role

Full Time (40 hours per week)

Exemption from Overtime

Salaried Exempt

Essential Supervisory Responsibilities

1. None

Essential Job Responsibilities

1. Study Design: Review study protocols to ensure execution plans are aligned with research objectives and best practices. Set up studies in electronic data capture systems. (Pathology studies).

2. Study Execution: Work closely across Virscio to manage study readouts to meet data delivery deadlines. Work closely with the Study Coordinator, Scientists, Study Directors and Functional Heads to organize and execute analyses in accordance with GLPs. Proactively organize protocols, results and templates to enable seamless information sharing and data integration.

3. Study Reporting: Review draft reports and tables to check for quality and accuracy. Work closely with Scientists, Technicians, Study Coordinators and Business Development to organize analyses and reporting in accordance with GLP and contractual obligations.

4. Regulatory & Administrative Support: Contribution and updating of SOPs. Contribute to maintenance of facility GLPs and AAALAC credentials.

5. Scientific Communications: Network with external colleagues to build confidence in our capabilities.

Qualifications

1. Education level/Certifications/Licensures

  • BS/BA degree in a relevant field required.

2. Experience

  • BS/BA and 5+ years' experience working in a pathology laboratory or molecular laboratory interacting with histologists and pathologists.
  • CRO experience preferred.
  • Working knowledge of histology lab processes, workflows, and reporting in GLP and non-GLP preclinical studies.
  • Experience working with Anatomic Pathology electronic data capture modules (Provantis, Concentriq, Visiopharm, etc.) including setting up individual studies, generating reports and tabulated data.

3. Specific competencies

  • Demonstrated proficient use of AI leading to process improvements and refinements in resource management.
  • Proficiency using business related (MS Office/Teams, Skype, Zoom, etc.) and pathology-specific (Provantis, Concentriq, Visiopharm, etc.) software systems.
  • Excellent verbal and written communication skills.
  • Strong self-discipline and ability to work productively with minimal supervision.
  • Strong collaboration skills, critical thinking and attention to detail.
  • Resourceful, enthusiastic, and collaborative.
  • Passionate about learning, testing novel approaches, and shaping the culture and future of Virscio.

4. Travel expectations

  • 5% Travel

Virscio logo

About Virscio

Sourced by ZipRecruiter

Industry

Biotechnology research and development

Company size

11 - 50 Employees

Headquarters location

New Haven, CT, US

Year founded

2002