Senior Clinical Supply Program Manager

AbbVie; North Chicago (IL); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Health insurance

401(k) plan

Paid time off

Job summary

AbbVie seeks a qualified professional to input to Clinical Study Teams, translating protocol designs into packaging and labeling sections. You will author protocol-specific labeling and create manufacturing and packaging work orders with vendors to ensure timely availability of clinical supplies.

You will participate in cross-functional initiatives, manage risks, and drive process improvements while ensuring compliance with global regulations and SOPs.

Qualifications

• Bachelor’s degree and 3 years in pharmaceutical industry preferred.
• Experience in Drug Discovery, Development, Clinical Operations, or Supply Chain.
• Proficient in applying Global Regulations and SOPs.
• Capable of cross-functional collaboration and multitasking under deadlines.

Responsibilities

• Translate clinical study design into packaging design and labeling sections.
• Create protocol-specific manufacturing and packaging work orders with vendors.
• Forecast protocol bulk drug product requirements and clinical supplies.
• Lead cross-functional initiatives and drive continuous improvement.

Skills

Project Management

Communication

Problem Solving

Collaboration

Time Management

Education

Bachelor’s Degree in physical sciences, math, engineering or pharmacy

Job description

AbbVie seeks a qualified professional to input to Clinical Study Teams, translating protocol designs into packaging and labeling sections. You will author protocol-specific labeling and create manufacturing and packaging work orders with vendors to ensure timely availability of clinical supplies.

You will participate in cross-functional initiatives, manage risks, and drive process improvements while ensuring compliance with global regulations and SOPs.