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Clinical Labeling Support Specialist
Sriven Systems Inc.North Chicago, IL🇺🇸United StatesPosted 4 Aug 2026
Quick Overview
Work Type
Hybrid
Level
Mid Senior
Job Description
Job Title: Clinical Labeling Support Specialist
Location: North Chicago, IL (Hybrid)
Duration: 12 Months
Job Summary
We are seeking a detail-oriented Clinical Labeling Support Specialist to support clinical labeling activities in a GMP-regulated environment. The role involves label creation, proofreading, documentation review, data entry, and coordination of labeling activities to ensure compliance with regulatory requirements.
Responsibilities
- Create and proofread clinical labels with a high degree of accuracy.
- Transfer labeling information into new systems.
- Review source documents, SOPs, and protocols.
- Support labeling documentation and approval processes.
- Maintain accurate records in a GMP-regulated environment.
- Coordinate with cross-functional teams on labeling activities.
- Handle multiple projects while meeting deadlines.
Required Skills
- Experience in clinical labeling, regulatory documentation, or document control.
- Strong proofreading and data entry skills.
- Knowledge of GMP/GxP environments.
- Excellent attention to detail.
- Strong computer skills and proficiency in Microsoft Excel.
- Ability to learn new systems quickly.
- Excellent communication and organizational skills.
Preferred Skills
- Experience with clinical trials or pharmaceutical labeling.
- Exposure to labeling systems or data migration.
- Adobe or labeling software experience.
Skills
Clinical Trials
Compliance
Data Entry
Microsoft Excel
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