ZipRecruiter

Log In

1

Clinical Labeling Specialist Jobs (NOW HIRING)

Exalta Group

Labeling Specialist

Bethlehem, PA · On-site

The Specialist will ensure adherence to company policy and procedures and will assist in ... and clinical performance (SSCPs), etc. * Ensures labeling documentation and labeling is ...

Exalta Group

Labeling Specialist

Marquette, MI · On-site

The Specialist will ensure adherence to company policy and procedures and will assist in ... and clinical performance (SSCPs), etc. * Ensures labeling documentation and labeling is ...

Exalta Group

Labeling Specialist

Marquette, MI · On-site

The Specialist will ensure adherence to company policy and procedures and will assist in ... and clinical performance (SSCPs), etc. * Ensures labeling documentation and labeling is ...

Teleflex

Labeling Specialist

Maple Grove, MN

Position Summary Teleflex is seeking a Labeling Specialist to join our Labeling department! The ... Partners with Regulatory Affairs, Quality, R&D, Packaging, Clinical, and Marketing teams to ...

Teleflex

Labeling Specialist

Maple Grove, MN · On-site

Position Summary Teleflex is seeking a Labeling Specialist to join our Labeling department! The ... Clinical, and Marketing teams to maintain real-time data in database/spreadsheet. • Manages ...

LGC Group

QA Labeling Specialist

Milford, MA · On-site

$82K/yr

Company Description LGC Clinical Diagnostics develops and manufactures a comprehensive portfolio of ... At LGC, we are looking for a dedicated QA Labeling Specialist to join our ambitious engineering ...

LGC Group

QA Labeling Specialist

Milford, MA

$55K/yr

Company Description LGC Clinical Diagnostics develops and manufactures a comprehensive portfolio of ... At LGC, we are looking for a dedicated QA Labeling Specialist to join our ambitious engineering ...

LGC Group

QA Labeling Specialist

Milford, MA · On-site

$82K/yr

Company Description LGC Clinical Diagnostics develops and manufactures a comprehensive portfolio of ... At LGC, we are looking for a dedicated QA Labeling Specialist to join our ambitious engineering ...

Catalent, Inc.

Label Specialist

Kansas City, MO · On-site

Position Summary We have an opportunity for a Label Specialist to join our team and support the ... High-school diploma or GED. * 0-3 years of clinical labeling experience. * Ability to communicate ...

System One

Clinical Supplies Specialist I

Alameda, CA · On-site

$27 - $32/hr

Prepare packaging and labeling requests, manage depot and site shipments, and monitor study drug inventory levels. * Assist in supply planning and forecasting to optimize clinical trial logistics.

next page

Showing results 1-20

All JobsManufacturing JobsProduct Manufacturing JobsProduction Line Worker JobsClinical Labeling Specialist Jobs

Clinical Labeling Specialist information

See salary details

$30K

$69.5K

$121K

How much do clinical labeling specialist jobs pay per year?

As of Sep 12, 2026, the average yearly pay for clinical labeling specialist in the United States is $69,454.00, according to ZipRecruiter salary data. Most workers in this role earn between $45,000.00 and $83,000.00 per year, depending on experience, location, and employer.

What is a clinical labeling specialist?

Clinical Labeling Specialists are professionals responsible for developing and managing the labeling content for pharmaceutical products, ensuring that all packaging and documentation comply with regulatory requirements. They collaborate with regulatory, medical, and legal teams to create accurate and clear labels, leaflets, and instructions for use. Their work helps ensure that healthcare professionals and patients have the correct information needed for the safe and effective use of medications.

What are the key skills and qualifications needed to thrive as a clinical labeling specialist?

To thrive as a Clinical Labeling Specialist, you need a solid understanding of regulatory requirements, scientific terminology, and labeling processes, typically supported by a degree in life sciences or a related field. Familiarity with regulatory submission systems, document management tools, and labeling software is essential. Attention to detail, strong written communication, and cross-functional collaboration are standout soft skills in this role. These competencies are crucial to ensure that clinical labeling is accurate, compliant, and effectively supports patient safety and regulatory approval.

How does a clinical labeling specialist collaborate with cross-functional teams during the drug development process?

As a Clinical Labeling Specialist, you work closely with regulatory affairs, clinical operations, medical writing, and quality assurance teams to ensure labeling documents meet international regulatory requirements. Collaboration typically involves participating in project meetings, reviewing and incorporating feedback on labeling content, and ensuring all safety and usage information is accurately reflected. This cross-functional teamwork is essential to maintain compliance and timely submission of labeling materials throughout the product lifecycle.

What cities are hiring for Clinical Labeling Specialist jobs?

Cities with the most Clinical Labeling Specialist job openings:

What are popular job titles related to Clinical Labeling Specialist jobs?

For Clinical Labeling Specialist jobs, the most frequently searched job titles are:

Infographic showing various Clinical Labeling Specialist job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $69,454 per year, or $33.4 per hour.

Clinical Labeling Specialist

Garden City, NY • On-site

CCL Label, Inc.
Plastics Packaging Film and Sheet (including Laminated) Manufacturing • 10K+ employees
Learn more about CCL Label, Inc.external

Full-time

Posted 23 days ago

Key responsibilities

  • Support daily label generation and production operations for clinical trial materials.

  • Prepare, print, review, document, and ship clinical labels in compliance with procedures and standards.

  • Monitor printing processes for quality issues and perform reprint activities as needed.

CCL Label rating

8.7

Company rating: 8.7 out of 10

Based on 21 frontline employees who took The Breakroom Quiz

Job description

CCL Clinical Systems is seeking a detail-oriented Clinical Labeling Specialist to support daily label generation and production operations for clinical trial materials. In this role, you will be responsible for preparing, printing, reviewing, documenting, and shipping clinical labels while ensuring compliance with company procedures, customer requirements, and quality standards.
The ideal candidate is highly organized, possesses strong attention to detail, and is comfortable working in a regulated production environment where accuracy and confidentiality are critical.
Key Responsibilities
  • Participate in pre-production reviews with the Project Leader.
  • Select and allocate appropriate label stock for production jobs.
  • Prepare production rooms and workstations for area clearance.
  • Print labels according to customer specifications and project requirements.
  • Monitor printing operations to identify and address quality issues, defects, or production concerns.
  • Perform reprint and integration activities for replacement labels as needed.
  • Prepare packaging labels and supporting materials.
  • Accurately document production activities and maintain required records throughout each run.
  • Review production documentation for completeness and accuracy before submitting to Quality Assurance (QA) for review and release.
  • Support shipping and fulfillment activities to meet customer requirements.
  • Assist with additional operational tasks as needed to support day-to-day business operations.

Qualifications & Requirements
  • High School Diploma or equivalent required.
  • Minimum 1 year of experience in clinical label production and clinical trial booklet production.
  • Experience working in a regulated manufacturing, pharmaceutical, biopharmaceutical, clinical research, or healthcare environment preferred.
  • Working knowledge of current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOPs).
  • Strong proofreading skills with the ability to review printed materials, labels, and production documentation for accuracy.
  • Ability to follow detailed verbal and written instructions and adhere to established procedures.
  • Strong attention to detail with a commitment to accuracy and quality.
  • Ability to maintain detailed production records and documentation in accordance with quality and compliance requirements.
  • Basic mathematical, grammatical, and computer skills.
  • Effective verbal and written communication skills.
  • Ability to identify and resolve production issues while maintaining quality standards.
  • Ability to work independently and collaboratively in a fast-paced production environment.
  • Demonstrated ability to handle confidential customer and clinical trial information with discretion and professionalism.

Work Environment
CCL Clinical Systems is committed to providing a clean, safe, and professional work environment for all employees. This position requires working in a production setting where attention to detail, quality, and compliance are essential.
Confidentiality
Due to the nature of our business, all customer-related clinical trial information is strictly confidential. Employees are required to maintain confidentiality and adhere to company policies regarding the protection of customer and clinical trial data.

What CCL Label employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply