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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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