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Data Review Scientist Jobs in Delaware (NOW HIRING)

Qnity

Senior Engineer / Scientist

Newark, DE

... and technical review meetings.This position isultimately intendedto be basedonsitein Newark ... Partner with research, applications, product development, manufacturing, and data science teams to ...

New

MSD

Senior Specialist, Quality Assurance

Wilmington, DE · On-site

$80K - $110K/yr

... data review/audit trail review instructions for users), disaster recovery plans, business ... Preferably in Science, Information Technology, Engineering or equivalent. Experience: * Hands-on ...

CCRM Fertility

Clinical Lab Technician

Newark, DE · On-site

$22 - $26/hr

... data review, and associated computer use. * Process samples according to Lab protocols for testing ... Bachelor of Science in Laboratory Sciences preferred. * 1+ years' experience in specimen processing ...

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All JobsData Review Scientist JobsData Review Scientist Jobs in Delaware

Data Review Scientist information

See Delaware salary details

$37.5K

$122.8K

$196.7K

How much do data review scientist jobs pay per year?

As of Aug 21, 2026, the average yearly pay for data review scientist in Delaware is $122,844.00, according to ZipRecruiter salary data. Most workers in this role earn between $98,600.00 and $136,100.00 per year, depending on experience, location, and employer.

What does a data review scientist do?

A Data Review Scientist is responsible for reviewing, validating, and interpreting scientific data to ensure its accuracy, integrity, and compliance with regulatory standards. They often work in pharmaceutical, clinical, or research settings, analyzing experimental or clinical trial data for errors, inconsistencies, and completeness. Their work helps ensure that scientific findings are reliable and can be used to support research conclusions or regulatory submissions.

What are the key skills and qualifications needed to thrive as a data review scientist?

To thrive as a Data Review Scientist, you need a solid background in life sciences or related fields, strong analytical skills, and experience with data validation and interpretation. Familiarity with data management systems such as LIMS, proficiency in statistical analysis tools like SAS or R, and knowledge of regulatory guidelines (e.g., GxP, FDA) are typically required. Attention to detail, critical thinking, and effective communication help ensure accuracy and clarity when reviewing complex datasets and collaborating with cross-functional teams. These skills are crucial for maintaining data integrity and supporting regulatory compliance in scientific research and clinical trials.

What are some common challenges faced by data review scientists when ensuring data integrity in research projects?

Data Review Scientists often encounter challenges such as identifying inconsistencies in large datasets, resolving discrepancies between source documents and digital records, and ensuring strict adherence to regulatory standards like GLP or GCP. They must also coordinate with cross-functional teams, including laboratory staff and data managers, to clarify data queries and implement corrective actions promptly. Staying updated with evolving data management technologies and regulatory requirements is crucial for success and helps maintain the highest levels of data integrity throughout research projects.

What is the difference between Data Review Scientist vs Data Analyst?

AspectData Review ScientistData Analyst
Required CredentialsBachelor's degree in data science, statistics, or related field; familiarity with data review toolsBachelor's degree in data analysis, statistics, or related field; proficiency in data visualization and analysis software
Work EnvironmentHealthcare, clinical trials, or research settings focusing on data quality and complianceBusiness, marketing, finance, or operations across various industries analyzing data trends
Employer & Industry UsagePharmaceutical companies, research institutions, healthcare organizationsCorporations, marketing agencies, financial firms, and tech companies

While both roles involve working with data, Data Review Scientists primarily focus on ensuring data quality and compliance in research or clinical settings, whereas Data Analysts interpret data to inform business decisions across diverse industries.

What are popular job titles related to Data Review Scientist jobs in Delaware?

For Data Review Scientist jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Data Review Scientist jobs in Delaware look for?

The top searched job categories for Data Review Scientist jobs in Delaware are:

What cities in Delaware are hiring for Data Review Scientist jobs?

Cities in Delaware with the most Data Review Scientist job openings:

Data Review Scientist jobs near you
Infographic showing various Data Review Scientist job openings in Delaware as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, and 4% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $122,844 per year, or $59.1 per hour.

Director, Clinical Research Scientist IAI

Incyte Corporation

Wilmington, DE • On-site

Other

Re-posted 23 days ago

Job description

Overview

Incyte is a biopharmaceutical company focused on the discovery development and commercialization of novel medicines to meet serious unmet medical needs in oncology and inflammation and autoimmunity. Incyte is committed to the rigorous pursuit of research and development excellence to improve the lives of patients make a difference in health care and build sustainable value.

The Company strives to discover and develop first-in-class and best-in-class medicines-advancing a diverse portfolio of large and small molecules.

Job Summary

The clinical scientist will provide scientific clinical and operational input to early and late-stage clinical development programs. This role will work on cross-functional study teams for the design execution and monitoring of clinical trials as well as assist with data interpretation and communication.

Key Responsibilities:

  • Development of protocols for clinical studies.
  • Contribute to the development of program strategy for assigned compounds/programs including participation in the preparation of clinical development plans
  • Drafting and review of clinical scientific documents such as IND amendments Investigator Brochures Annual Reports and other Health Authority submissions.
  • Monitor review and summarize safety and efficacy data in ongoing studies.
  • Represent clinical development on project teams.
  • Develop relationships with appropriate consultants and external experts and utilize these relationships to obtain feedback on protocol design.
  • Clinical lead for study abstracts posters oral presentations and manuscripts for assigned studies.
  • Serve as liaison to project teams, CROs, Clinical sub-teams and others.
  • Maintain updated knowledge of competitive landscape in regard to assets with similar MOA and/or evolving standards of care for indications of interest.

Qualifications:

  • Degree in scientific/life-sciences. Pharm.D. or Ph.D. preferred.
  • Minimum of 5 years of drug development experience are required. Alternative drug development experience will be considered.
  • Prior Dermatology or immunology experience is preferred.
  • Ability to work independently multi-task and work in a fast-paced environment.
  • Excellent written and oral communication skills.
  • Strong Analytical ability.
  • Ability to accommodate up to 20% travel or as business dictates

Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.

Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer.

We Respect Your Privacy

Learn more at:http://www.incyte.com/privacy-policy

The Incyte hiring organization processes your personal data to manage your job application in order to enter into an employment relationship with you if you are the successful candidate.

During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job. You can learn more about this process here.

You may have the right to access, delete, restrict, edit, move, or object to the use of your personal data. You may also have a right to report concerns to the authority responsible for data privacy in the country where the position is based or where you live or work.

You can learn more about Incyte's data protection practiceshere. By accessing this link you can learn about the types of personal data we collect, how we use it, whether collection and processing is optional, sources of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incyte's data protection officer, and your supervisory authority (if applicable).

Please contact privacy@incyte.com if you have any questions or concerns or would like to exercise your rights.

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