# Clinical Trial Material Manager (2nd Shift)

**Company**: IQVIA Laboratories
**Location**: Marietta, GA
**Work arrangement**: onsite
**Experience**: senior
**Job type**: full-time
**Salary**: $77,700.00 - $161,800.00
**Category**: Operations
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Marietta-Georgia-United-States-of-America/Clinical-Trial-Material-Manager--2nd-Shift-_R1552456?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_eea788a8-c17

## Description

We are seeking a Clinical Trial Material Manager (2nd Shift) to join IQVIA Laboratories at Marietta, GA.

The Clinical Trial Material Manager leads daily second-shift (2:00 PM to 11:00 PM) manufacturing operations in a regulated, high-volume production environment. This role ensures on-time delivery, quality compliance, staff performance, and continuous improvement while partnering across Project Services, Warehouse, Logistics, Quality, and IT.

**Responsibilities**

- Lead, coach, and develop a team of direct reports in a dynamic production environment

- Manage daily and long-range production schedules to meet customer demand and service-level production targets

- Prioritize urgent, same-day, and future-dated work orders to ensure on-time delivery

- Coordinate daily with Project Management, Warehouse, Logistics, Quality, and IT to resolve production issues and prevent delays

- Utilize LIMS to support production files, platform reports, production metrics, dashboards, and compliance reporting

- Perform root cause investigations for quality incidents, customer complaints, operations incidents, and in-process deviations

- Lead and support Lean, Six Sigma, and process improvement initiatives to optimize production flow and reduce bottlenecks

**Requirements**

- Bachelor’s degree, 10 years of experience in lieu of degree

- Minimum 5 years of people management experience, managing 20 employees in a manufacturing environment

- Minimum 5 years of experience managing manual assembly or production lines

- Minimum 2 years of experience leading process improvement projects

- Working knowledge of Microsoft Excel, Outlook, and PowerPoint

- Working knowledge of ICH, GMP, and OSHA regulations

- Six Sigma Yellow or Green Belt experience required; certification preferred

**Knowledge, Skills and Abilities**

- Strong leadership, coaching, and staff development skills in a high-volume production environment

- Ability to prioritize urgent and business-critical work while maintaining quality and compliance expectations

- Effective cross-functional communication skills with the ability to escalate risks, constraints, and operational performance updates

- Strong problem-solving skills with the ability to conduct investigations and drive root cause analysis

- Ability to support overtime, weekends, and holidays based on critical business needs and accelerated trial timelines

**What We Offer**

- Competitive salary: $77,700.00 - $161,800.00 per year

- Comprehensive benefits program, including physical, mental and emotional, financial and social well-being resources

## Skills

### Required
- Microsoft Excel
- Outlook
- PowerPoint
- LIMS
- ICH
- GMP
- OSHA
- Six Sigma

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Marietta-Georgia-United-States-of-America/Clinical-Trial-Material-Manager--2nd-Shift-_R1552456?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)