Senior Project Coordinator, Clinical Supply

  • AbbVie, Inc
  • North Chicago, Illinois
  • Full Time

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

Purpose: Serves as a primary contract for project management of key Clinical Supply Chain documentation, tasks, and packaging activities in a GMP environment. Owns and supports readiness activities for clinical supply packaging operations. Owns inventory management system set up activities required to drive clinical supply packaging operations.

Responsibilities

  • Ensures system set up components are available on time to support Clinical Packaging Production as needed. Owns design, creation, and approval processes for inventory management system activities
  • Identify and lead opportunities for process improvements within and cross functions. Responsible for creating and maintaining processes and procedures related to group activities.
  • Extract job specific information from planning system to independently create protocol-specific packaging work orders. Serves as primary representative for packaging job readiness in all packaging operations meetings.
  • Act as a key interface between project management group, packaging operations, and QA, influencing when needed to ensure packaging activities are set up appropriately and efficiently
  • Identifies, develops, communicates and tracks task completion dates, activities, logistics, and milestones in support of CSPMs to ensure the timely availability of investigational drug supplies.
  • Serves as trainer to newer team members for all job responsibilities. Develop and maintain up-to-date Training Module for Center of Excellence. Review and update training matrix for all departmental employees as required.
  • Translates stability and pre-packaging requests into an executed packaging design. Owns complete process from system set-up, to work order requests, to material transfers, as needed.

Qualifications

  • Bachelor's degree in the Life or Physical Sciences preferred. Will consider Business Administration, Math or Engineering with appropriate work experience.
  • 3-5 total years of Pharmaceutical or Biotechnology industry or equivalent experience preferred.
  • Must possess a thorough understanding of the overall clinical drug supply chain in a global operating enterprise.
  • Knowledge of regulations and standard affecting pharmaceutical products (i.e., CFR210/211, cGMP, etc.) is preferred
  • Must have excellent problem solving and logical reasoning skills.
  • Proactive approach to problem solving, thinking outside of the box, and ability to identify creative solutions to unique problems.
  • Must be prepared to continually recognize the needs of Materials Management customers, prioritize as necessary, and trouble shoot abnormal or challenging situations.
  • Proficient with standard computer software. Must be able to effectively manage multiple projects at one time.
  • Strong Project Management skills.
  • Strong communication skills (both written and oral). Ability to work independently or with a group.

Additional Information

Applicable only to applicants

Job ID: 480728669
Originally Posted on: 6/11/2025

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