​​Senior Manager, Planning and Production Solution​s--Global Clinical Supply Operations

Pfizer

Hybrid

Quick summary

Work type
Hybrid
Location
Groton, CT
Salary
$124,400–$207,400 / yr
Posted
4 days ago
Closes
Jun 26, 2026

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $183k
This role $166k
$113k most similar roles pay here $229k

This role pays less than 74% of similar roles. Most pay $165,000–$201,750 — the shaded band above. At the midpoint, this role pays about $166k versus about $183k for comparable roles.

Based on 238 similar postings.

Employer

About Pfizer

Pfizer Inc. is one of the world''s largest biopharmaceutical companies, researching, developing, manufacturing, and marketing medicines and vaccines across multiple therapeutic areas including oncology, cardiology, and infectious diseases. Industry: Biopharmaceuticals

Pfizer currently has 33 open roles on FindRole.

Listed pay typically runs $124,400–$207,400 across 33 roles with salary data.

Most-posted roles

View all roles at Pfizer

At a glance

TL;DR · ​​Senior Manager, Planning and Production Solution​s--Global Clinical Supply Operations

As a Senior Manager in Clinical Packaging and Labeling Systems (PPS) within Pfizer’s Global Clinical Supply Operations team, you will oversee the design, production, and delivery of high-quality labels for clinical studies while ensuring compliance with GMP and regulatory standards. Your day-to-day responsibilities include managing label creation and inventory systems such as PRISYM360 and EMD365, driving operational strategies to enhance efficiency, and collaborating with internal teams and external vendors to execute packaging and distribution activities. You will also develop metrics for operational reporting, monitor regulatory requirements, and implement new technologies to improve traceability and identification of clinical trial supplies. The role requires expertise in PRISYM360, Phrase Library administration, and other labelling systems, along with strong project management skills and experience in complex clinical study designs.

What you'll do

  • Ensure compliance with GMP and regulatory requirements in label design and production.
  • Oversee end-to-end execution of labeling activities using PRISYM360 and other systems.
  • Lead the implementation of new global standards to enhance identification and traceability.
  • Continuously evaluate and improve processes for operational efficiency and quality.
  • Develop and support metrics and KPIs for data accuracy and inspection readiness.

What we're looking for

  • At least 5 years of clinical supply operations experience
  • Proficiency in PRISYM360 and other labelling systems
  • Strong knowledge of GMP documentation and regulatory requirements
  • Experience with complex clinical study designs and project management
  • Excellent communication, negotiation, and presentation skills
  • Familiarity with Microsoft Office programs and supply chain enterprise systems
  • Lean or Six Sigma training preferred

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