> Markdown version of [/jobs/ext/3595260-associate-scientist-data-reviewer](https://www.wearedevelopers.com/jobs/ext/3595260-associate-scientist-data-reviewer). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md).

---

# Associate Scientist / Data Reviewer

- **Company:** GL STAFFING SERVICES, INC.
- **Location:** Fort Lauderdale, FL, United States
- **Experience:** Experienced
- **Salary:** $72,800.0 - $83,200.0
- **Contract:** Permanent contract
- **Skills:** Microsoft Word, Microsoft Excel, Data Analysis, Data Validation, Data Integrity, Document Management Systems, Microsoft PowerPoint, Technical Data Management Systems
- **Published:** October 6, 2026
- **Apply:** https://www.thejobnetwork.com/job/d4c6bab8-d979-4418-ae65-4ccf1dcbb4ee/data-analyst

## About the Role

This is an excellent opportunity for a scientific professional with experience in a cGMP-regulated pharmaceutical, analytical, laboratory, or R&D environment who has strong attention to detail and an interest in data review, documentation, and pharmaceutical product development., * Bachelor's degree in Chemistry, Chemical Engineering, Pharmacy, Forensic Science, Pharmaceutical Sciences, or a related scientific discipline.

 * 3+ years of experience in a cGMP-regulated environment within pharmaceutical, analytical, laboratory, R&D, QC, or a related discipline.
 * Familiarity with analytical laboratory methodologies and practices.
 * Familiarity with laboratory instrumentation such as:
 * HPLC / UPLC
 * UV-Vis
 * GC
 * Other common analytical laboratory equipment
 * Strong understanding of laboratory documentation and data review practices.
 * Strong attention to detail and ability to identify discrepancies or inconsistencies in scientific data and documentation.
 * Strong organizational skills with the ability to manage multiple priorities and deadlines in a fast-paced environment.
 * Proficiency in Microsoft Excel, Word, and PowerPoint.
 * Strong written and verbal communication skills in English.
 * Ability to work effectively both independently and as part of a cross-functional team.

Preferred Qualifications

 * Experience with electronic document management systems.
 * Experience reviewing analytical laboratory data in a pharmaceutical or cGMP environment.
 * Experience with data integrity principles and laboratory documentation practices.
 * Familiarity with statistical analysis or scientific data-analysis applications.
 * Familiarity with pharmaceutical manufacturing or laboratory process equipment, such as liquid manufacturing equipment or powder blenders.
 * Experience supporting QA review, document control, QC, analytical development, or R&D activities.
 * Experience preparing scientific reports, data summaries, charts, or visualizations.

## Description

We are seeking three Associate Scientists / Data Reviewers to support pharmaceutical product development activities within a regulated R&D environment.

This role is responsible for technical data review, data verification, documentation review, and data integrity activities prior to submission of R&D records to Quality Assurance (QA) for review and release., * Conduct technical review of R&D laboratory data and supporting documentation.

 * Verify data for accuracy, completeness, consistency, and integrity prior to submission to QA.
 * Review laboratory records, analytical results, calculations, and supporting documentation for compliance with applicable procedures.
 * Identify discrepancies, missing information, documentation issues, and potential data integrity concerns.
 * Work with laboratory and R&D personnel to resolve documentation and data-related issues.
 * Ensure R&D records meet applicable technical and quality requirements before QA review and release.

Documentation & Reporting

 * Organize, maintain, and control documentation and records associated with R&D product development activities.
 * Review technical documents and laboratory records for completeness and accuracy.
 * Draft summary reports based on laboratory and R&D data.
 * Prepare charts, tables, graphs, and other visual representations of scientific data.
 * Maintain appropriate documentation in accordance with SOPs and applicable quality requirements.
 * Upload and maintain R&D documents within electronic document management systems.
 * Ensure documentation is properly organized, traceable, and readily accessible.

Project & Team Support

 * Coordinate routine project activities, documentation, materials, and communications with internal teams and external partners.
 * Participate in project and team meetings and maintain accurate meeting records.
 * Track assigned action items and follow up to ensure timely completion.
 * Support project timelines and contribute proactively to team objectives.
 * Work collaboratively with R&D, analytical laboratory, QA, and other cross-functional teams.
 * Build and maintain effective working relationships with internal colleagues and external partners.

Compliance & Quality

 * Perform all activities in accordance with applicable SOPs, quality standards, and company procedures.
 * Maintain a strong focus on data integrity, documentation accuracy, and compliance.
 * Support a culture of quality and continuous improvement within the R&D organization.
 * Follow applicable cGMP requirements and laboratory documentation practices.
 * Perform other duties and responsibilities as assigned.