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Scientific Data Curator Jobs (NOW HIRING)

MIT Lincoln Laboratory

Data Scientist

Lexington, MA · On-site

The position will involve leading the development of AI/ML models, data curation, planning and conducting field data collections, leading small programs, collaborating with other scientists and ...

MIT Lincoln Laboratory

Data Scientist

Lexington, MA · On-site

The position will involve leading the development of AI/ML models, data curation, planning and conducting field data collections, leading small programs, collaborating with other scientists and ...

MIT Lincoln Laboratory

Data Scientist

Lexington, MA

The position will involve leading the development of AI/ML models, data curation, planning and conducting field data collections, leading small programs, collaborating with other scientists and ...

Xforia, Inc.

Data Steward

... and curation teams. This role requires a deep understanding of: • Logical data modeling • ... science, engineering, statistics, economics, or MBA • Bring 3+ years of experience in data ...

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How much do scientific data curator jobs pay per year?

As of Jul 7, 2026, the average yearly pay for scientific data curator in the United States is $72,627.00, according to ZipRecruiter salary data. Most workers in this role earn between $50,000.00 and $94,000.00 per year, depending on experience, location, and employer.

What are the typical daily responsibilities of a Scientific Data Curator?

As a Scientific Data Curator, your daily tasks often include reviewing and validating scientific datasets, annotating data with relevant metadata, and ensuring that datasets comply with established data standards and best practices. You may work closely with researchers to interpret data requirements, resolve inconsistencies, and document curation processes thoroughly. Collaboration with computational scientists, biostatisticians, and IT teams is common, especially when integrating new data sources or improving database functionalities. These responsibilities help maintain the quality and usability of data resources, which are vital for ongoing research projects and publications.

What is a Scientific Data Curator job?

A Scientific Data Curator is responsible for collecting, organizing, annotating, and maintaining scientific datasets to ensure they are accurate, accessible, and reusable. They work with researchers to standardize data formats, apply metadata standards, and manage databases or repositories. This role is essential in fields like bioinformatics, genomics, and environmental science, where large volumes of data must be carefully managed. Scientific Data Curators also ensure compliance with data-sharing policies and promote reproducibility in research by facilitating proper data documentation and preservation.

What are the key skills and qualifications needed to thrive in the Scientific Data Curator position, and why are they important?

A Scientific Data Curator needs a strong background in life sciences or related fields, combined with expertise in data management, data standards, and metadata annotation. Proficiency with bioinformatics tools, database management systems (like SQL), and experience with data curation software and FAIR data principles are highly valued, as are certifications in data science or information management. Attention to detail, strong organizational skills, and effective communication enhance collaboration with scientists, data engineers, and other stakeholders. These skills ensure accurate, accessible, and high-quality data that support research integrity and scientific discovery.

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What cities are hiring for Scientific Data Curator jobs? Cities with the most Scientific Data Curator job openings:
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Scientific Data Curator jobs near you
Infographic showing various Scientific Data Curator job openings in the United States as of July 2026, with employment types broken down into 1% Locum Tenens, 66% As Needed, 4% Full Time, 1% Part Time, 27% Nights, and 1% Summer. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $72,627 per year, or $34.9 per hour.
Protocol Data Analyst I

Protocol Data Analyst I

Edj Associates, Inc.

Washington, DC • On-site

Full-time

Re-posted 13 days ago

Job description


CONTINGENT HIRE NOTICE: This position is a contingent hire. Employment is contingent upon EDJ Associates, Inc. receiving a contract award. This position is performed primarily on-site at NIH headquarters in Bethesda, Maryland. Applicants must be able to obtain and maintain a security clearance from the federal government.
The Protocol Data Analyst I is part of the core abstraction team within the CTRO, responsible for processing new trial and amendment submissions within the 10-business-day service-level agreement (SLA). This role codes clinical trials using the NCI Thesaurus, abstracts biomarkers, processes accrual data, and supports person and organization curation in the Clinical Trials Reporting Program (CTRP) database.
        Process new trial registrations and amendments within the 10-business-day SLA, including reviewing submissions and notifying submitters of acceptance, rejection, or on-hold status.
        Abstract clinical trial administrative and scientific data following established SOPs.
        Code trials using the NCI Thesaurus terminology for disease/condition, intervention, biomarker, and anatomic site data elements.
        Process and validate accrual submissions, including verifying requestor associations and trial registration status.
        Support person and organization curation to ensure data consistency and quality.
        Review header information, protocol documents, and administrative data elements for each trial.
        Follow Good Clinical Practices (GCP) data-handling procedures and guidelines.
        Respond to user inquiries and assist with issue resolution through the ServiceNow ticketing system.
        Participate in the review of clinical research protocols, reports, and statistical analysis plans.
        Support quality assurance and data integrity activities as directed.
        Minimum of one (1) year of experience working in a clinical environment, including medical and regulatory technical writing/editing.
        Knowledge of drug and disease terminology.
        Strong attention to detail and commitment to data accuracy.
        Ability to follow standard operating procedures and work within defined timelines.
        Familiarity with GCP guidelines preferred.
        Ability to obtain and maintain a Level 1 (Non-Sensitive) NACI background investigation.

Tools and Technologies:

        Microsoft Office Suite (Word, Excel, PowerPoint)
        CTRP Registration and Protocol Abstraction systems
        NCI Thesaurus / Enterprise Vocabulary Services (EVS)
        ServiceNow or similar ticketing systems

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