Project Manager – Clinical Supply

SOKOL GxP Services

. Manage multiple clinical supply packaging and labeling projects, tracking schedules, milestones, and delivery commitments.

Posted 11/3/2026full-timeNew Brunswick • New Jersey • United StatesMid-LevelSenior💰 $91,603 - $116,355 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in managing clinical supply packaging and labeling projects while ensuring compliance with cGMP regulations. Proficient in SAP for executing transactions and maintaining project documentation, with strong project management and communication skills.

Highest-signal resume keywords

Clinical Supply ManagementSAP Transaction ExecutionProject ManagementGMP Regulatory CompliancePackaging and Labeling Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ExperiencePackaging and Labeling OperationsBills of Materials (BOMs)Process OrdersERP SystemsCGMP ComplianceDeviation and Change ControlDocumentation AuthoringMicrosoft Office 365Supply Chain Principles

Soft Skills

Written CommunicationVerbal CommunicationDecision-MakingOrganizational SkillsInfluencing Project Outcomes

Tools & Technologies

SAP

Industry Keywords

Pharmaceutical IndustryHealthcare ExperienceRegulatory ComplianceQuality AssuranceProject Tracking

Tech Stack

Tools & technologies

ERP

About the role

Key responsibilities & impact

Manage multiple clinical supply packaging and labeling projects, tracking schedules, milestones, and delivery commitments.
Coordinate drug products, packaging components, label text, randomization files, and other project deliverables.
Create and release Bills of Materials (BOMs) and production/process orders in SAP.
Execute SAP transactions, including goods receipt, goods consumption, and technical completion (TECO).
Review packaging and labeling specifications, vendor label proofs, production orders, and change orders.
Coordinate with Quality Assurance to support batch record documentation and release of finished clinical supplies.
Maintain cGMP and regulatory compliance, support deviation and change control activities, and contribute to process improvements.
Author and review procedural documentation.

Requirements

What you’ll need

Bachelor's degree or equivalent in pharmacy, engineering, business, or life sciences.
At least 3 years of experience in a GMP-regulated environment.
At least 3 years of clinical trial or packaging/labeling experience.
At least 3 years of Microsoft Office 365 experience.
Experience with ERP systems, such as SAP.
Strong project management skills, including managing multiple projects and critical timelines.
Strong written and verbal communication, decision-making, and organizational skills.
Knowledge of ERP/MRP systems and supply chain principles.
Authorization to work in the United States without visa sponsorship.
Preferred: 5–7 years of relevant pharmaceutical industry or related healthcare experience.
Preferred: Clinical supply or clinical trial experience.
Preferred: Experience with clinical packaging and labeling operations.
Preferred: Experience with SAP Bills of Materials, process orders, and related transactions.
Preferred: Ability to communicate effectively across teams and influence project outcomes.

Benefits

Comp & perks

Health insurance with dental and vision insurance options.
Holiday pay.
401(k) program.
Employee referral bonus program.
The client retains the right to hire the contractor directly.