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Research Associate (In-vitro Biology
Job in
Groton, New London County, Connecticut, 06349, USA
Listed on 2026-08-17
Listing for:
Pharmaceutical Company
Full Time
position Listed on 2026-08-17
Job specializations:
-
Research/Development
Biotech Research, Clinical Research, Research Scientist
Job Description & How to Apply Below
We are seeking an External Screening & In Vitro Biology Associate to support external screening programs, plate-based assay workflows, scientific data operations, and CRO/vendor coordination.
This role will work closely with internal scientists, cross-functional teams, and external research partners to ensure screening requests are executed efficiently and that high-quality, accurate data is delivered on time.
Key Responsibilities- Manage and maintain external screening data, vendor portals, project records, and screening repositories
. - Process screening requests and review, validate, QC, format, and distribute screening data to internal scientists.
- Coordinate with CROs and external vendors to track screening requests, deliverables, timelines, and data issues.
- Support plate-based in vitro screening and assay transfer activities by organizing protocols, assay data, controls, and supporting documentation.
- Load and publish screening data using standardized templates and data-loading tools.
- Maintain vendor profiles, project information, screening protocols, and reference/control compound lists.
- Coordinate registration of new control/reference compounds when needed.
- Ensure data handling, documentation, and workflows follow established standards and are audit-ready.
- Collaborate with scientists and stakeholders to troubleshoot workflow and data-related issues.
- Support process improvements and additional screening/data operations activities as business needs evolve.
- Bachelor's degree in Biology or a related scientific discipline.
- Experience with scientific data workflows, data management, and data QC in a research, pharmaceutical, biotech, or screening environment.
- Experience with in vitro biology, pharmacology, high-throughput screening, or plate-based assay workflows preferred.
- Experience working with CROs, vendors, or external research partners is a plus.
- Strong attention to detail and ability to manage multiple projects and priorities.
- Strong organizational, communication, problem-solving, and documentation skills.
- Comfortable working in a fast-paced, cross-functional research environment
. - Ability to learn new scientific systems, data tools, and workflows quickly.
Position Requirements
10+ Years
work experience
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