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Project Manager - Pharma

Job

Skill

East Hanover, NJ (In Person)

$89,976 Salary, Full-Time

Posted 6 days ago (Updated 2 hours ago) • Actively hiring

Expires 7/3/2026

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Job Description

Project Manager - Pharma Skill United States, Jersey, East Hanover May 28, 2026
Overview Placement Type:
Temp to
Perm Salary:
$85,000-90,000
Salary Start Date:
Jun 29, 2026 Aquent Studios at our Pharmaceutical client is a custom-built agency partnership that provides scalability with world class talent to Novartis' in-house Materials Approval Process team. This collaboration creates exciting opportunities to work with Aquent Studios at one of the most admired pharmaceutical companies in the world. Focus on planning to drive operational excellence in the Material Approval Process (MAP) executing on E2E critical tasks to compliantly advance the in and above brand commercial assets from submission to compliant withdrawal from the Digital Asset Management system (DAM) and the Market. Major Activities Lead MAP for
Urgent PR, Market Access, Training, Communications, and NPS Submissions:
Review assets for readiness, ensure the MAP metadata is accurate, and triage to appropriate reviewers in accordance with Tiered Review process, published guidance documents, and WPDs. Understand, articulate, and execute specific deliverables critical to MAP capacity and resource planning with agility to pivot based on business dynamics. Own projects by navigating obstacles, seeking stakeholder input, and presenting options with recommendations.
Inventory Management:
Collaborate with Content Owners (CO), and lead system workflows to ensure all commercial materials are proactively expired as required and ensure compliance by validating that assets are removed from Market no later than expiration/withdrawal from the DAM.
Project Management:
Collaborate cross-functionally to drive creation and maintenance of MAP Forecasts to ensure appropriate planning and progress of all brand deliverables for Launches, Label Updates, CORE triggers, Campaigns, Congresses, and Events. Ensure MAP workflows are followed to drive efficient review process while aligned with compliance standards. Active participant in weekly agency status and MAP meetings, to ensure all projects are on track.
Process and System:
Troubleshoot system challenges for internal and external partners. As technologies evolve, provide solutions, guidance, and best practices to all users. Identify optimization opportunities based on observations, system user experience, and agency technology advancements.
Ideal Background Minimum requirements:
Education (minimum/desirable):
  • 4-Year degree.
Focus in Business, Marketing, or Communications preferred.
Experience/Professional Requirements:
  • 2+ years' experience in pharmaceutical advertising, marketing, communications, digital/content strategy
  • Functional experience in pharmaceutical marketing operations, preferred
  • Working knowledge of FDA and Pharmaceutical regulatory and compliance guidelines for advertising and promotion
  • Understanding of pharmaceutical review and approval process preferred
  • Project Management skills
  • Proficiency in computer applications, including Microsoft 365, Adobe Acrobat, and Content Review software (Aprimo Marketing Studio a plus) with excellent meeting hygiene, data organization, and clear accountability #LI-JH5