Director, Portfolio Program Management

AbbVie

Confirmed live 2 days ago High trust

Quick summary

Work type
On-site
Location
Irvine, CA
Salary
$160,500–$305,000 / yr
Posted
45 days ago
Freshness
Confirmed live 2 days ago
Closes
Jul 28, 2126

Market check

Salary context

Above market

How this pay compares to similar roles

Similar $203k
This role $233k
$137k most similar roles pay here $323k

This role pays more than 68% of similar roles. Most pay $159,906–$246,700 — the shaded band above. At the midpoint, this role pays about $233k versus about $203k for comparable roles.

Based on 240 similar postings.

Employer

About AbbVie

AbbVie is a global biopharmaceutical company focused on discovering and delivering innovative medicines and solutions in immunology, oncology, neuroscience, and eye care. Its products include Humira, Skyrizi, and Rinvoq.

AbbVie currently has 297 open roles on FindRole.

Listed pay typically runs $109,500–$208,500 across 271 roles with salary data.

Most-posted roles

View all roles at AbbVie

At a glance

TL;DR · Director, Portfolio Program Management

The Director, Portfolio Program Management serves as an operational leader within the Aesthetics Medicine division, partnering with asset strategy leaders and project managers to drive execution across the product portfolio. This role involves managing complex programs for new pharmaceutical products, clinical indications, and global expansions of existing products. Day-to-day responsibilities include developing cross-functional plans, monitoring budgets and milestones, facilitating team meetings, and performing risk mitigation. The candidate will utilize enterprise-level project management tools, Gantt charts, decision trees, and forecasting techniques to ensure alignment with approved asset strategies. Key requirements include a Bachelor or Master of Science in Pharmaceutical Sciences or a related field, along with extensive experience in pharmaceutical product development, regulatory affairs, and clinical development. Essential competencies include expert knowledge of global drug registration processes, proactive issue resolution, and the ability to lead multi-disciplinary teams across global locations.

What you'll do

  • Develop and execute global strategies for the development and launch of new pharmaceutical products and clinical indications.
  • Manage cross-functional project plans, including timelines, budgets, milestones, and resource allocation to ensure on-time delivery.
  • Identify, monitor, and mitigate project risks while resolving issues related to timing, resources, and funding.
  • Facilitate team meetings by setting agendas, capturing action items, and ensuring clear communication of management decisions.
  • Provide decision analysis expertise to help teams establish go/no-go criteria and make informed strategic choices.
  • Train and coach team members on project governance, planning processes, and the use of project management tools.
  • Report project progress, milestones, and forecasts to senior management and stakeholders across global locations.

What we're looking for

  • Bachelor of Science or Master of Science in Pharmaceutical Sciences or a related field is required.
  • 8 to 12 years of experience in the pharmaceutical industry in Clinical Development, Regulatory Affairs, Commercial, or Pharmaceutical Development areas are required.
  • At least 5 years of direct experience in Project Management for drug or device product development projects is required.
  • Advanced knowledge of global drug development, product registration, and launch processes is required.
  • Expert proficiency in project management software and portfolio management systems is required.
  • Exceptional written and oral communication skills to engage with diverse stakeholders are required.
  • Proven ability to manage risk, resolve issues, and facilitate team decision-making is required.
  • PMP certification is helpful but not required.

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