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VI

Scientific Research Associate

VIRSCIO, INC.·New Haven, Connecticut

Full Time·Hybrid·5-10 yrs·Posted 23 hours ago
Practice for this role

About the role

The Scientific Research Associate will manage study protocols, electronic data capture systems, and study scheduling to ensure data integrity and timely delivery. They will also collaborate with cross-functional teams to review reports, maintain GLP compliance, and support facility credentials.

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.

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

Requirements

Candidates must hold a Bachelor's degree and possess at least 5 years of experience in a pathology or molecular laboratory setting. Proficiency in histology workflows, GLP standards, and electronic data capture systems like Provantis is required.

  • bachelor degree
  • Attention To Detail
  • Quality Assurance
  • Communication Skills
  • Collaboration
  • Data Management
  • Critical Thinking
  • Resource Management
  • SOP Development
  • Pathology
  • Molecular Biology
  • GLP Compliance
  • Histology
  • Electronic Data Capture
  • Report Drafting
  • Study Protocols
  • Provantis

Posting details

Employment type
Full Time
Work arrangement
Hybrid
Experience
5-10 yrs
Location
New Haven, Connecticut
Posted
Jul 28, 2026
Application
Employer website
VI

Hiring organization

VIRSCIO, INC.

Virscio is a specialty translational research organization developing and providing innovative in vivo disease modeling and related preclinical research and development services to meet the preclinical, translational, and regulatory research needs of the pharmaceutical and life...

IndustryBiotechnology Research
TypePrivately Held
Size51-200 employees
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Market context

Connecticut research associate roles stay specialized

In Connecticut, Scientific Research Associate roles are typically competitive because employers look for candidates with both a bachelor’s degree and several years of pathology or molecular lab experience. Strong histology workflow knowledge, GLP familiarity, and hands-on use of electronic data capture systems such as Provantis can help you stand out. On this platform, job requirements and benefits are AI-summarized from the original posting, saving you time when comparing roles; review the summary for exact lab systems and compliance expectations before applying.

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