Scientific Support

The Fountain Group; Shrewsbury (MA); On-site; USD 26,000 - 34,000; Full time

Job summary

The Fountain Group is seeking a Data Review / Laboratory Technician to support GLP-compliant data handling and study documentation. The role involves reviewing paper and electronic data, verifying entries, and coordinating corrections with laboratory staff.

Responsibilities include archiving records, assisting in form/document revisions, supporting routine lab activities, and ensuring compliance with GLP/SOP standards. High attention to detail and strong Excel/Word skills are required.

Qualifications

• Must have knowledge of GLP and SOP requirements for study data documentation and review.
• Ability to review paper and electronic laboratory/study records for accuracy and completeness.
• Basic understanding of scientific data collection, documentation, and correction practices.

Responsibilities

• Review paper and electronic study data for completeness, accuracy, and GLP/SOP compliance.
• Verify data entries, corrections, forms, and electronic records against procedures and regulatory requirements.
• Identify data discrepancies and coordinate corrections with operational staff.
• Interact with Scientists, QA, and department personnel regarding study data and documentation issues.
• Archive, collate, organize, and maintain completed study records and documentation.
• Assist with preparation and revision of department forms and data-review documentation.
• Support basic laboratory activities, including inventory management, consumables/reagent handling, equipment operation, and routine laboratory documentation.
• Perform work in accordance with GLP regulations and SOPs.

Skills

GLP/SOP compliance

Data review

Attention to detail

Documentation management

Education

High school diploma or GED

Associate degree preferred

Tools

Microsoft Word

Excel

Job description

Data Review / Laboratory Technician
Location: Not specified
Pay Rate: $22/hr
Duration: 1 year

Job Description

• Review paper and electronic study data for completeness, accuracy, and GLP/SOP compliance.

• Verify data entries, corrections, forms, and electronic records against applicable procedures and regulatory requirements.

• Identify data discrepancies and coordinate appropriate corrections with operational staff.

• Interact with Scientists, QA, and department personnel regarding study data and documentation issues.

• Archive, collate, organize, and maintain completed study records and documentation.

• Assist with preparation and revision of department forms and data-review documentation.

• Support basic laboratory activities, including inventory management, consumables/reagent handling, equipment operation, and routine laboratory documentation.

• Perform work in accordance with GLP regulations and SOPs.

Education

• High school diploma or GED required.

• Associate degree preferred.

Required Skills

• Experience or knowledge of GLP and SOP requirements for study data documentation and review.

• Ability to review paper and electronic laboratory/study records for accuracy and completeness.

• Basic understanding of scientific data collection, documentation, and correction practices.

• Basic understanding of algebraic mathematics and scientific concepts.

• Proficiency with Microsoft Word and Excel.

• Ability to maintain organized laboratory and study documentation.

Preferred Skills

• Experience in a laboratory, research, pharmaceutical, biotechnology, or regulated environment.

• Familiarity with FDA GLP/GCP requirements and regulated study documentation.

• Experience with electronic data review and laboratory record systems.

• Experience handling laboratory consumables, reagents, inventory, and basic laboratory equipment.