Integrated Project Management

Consultant, Pharmaceutical Development and Commercialization

Integrated Project Management$125K — $180K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 8-15+ years of pharmaceutical industry experience in leading product development and commercialization projects.
  • Minimum 3 years in project or program management, with cross-functional leadership.
  • Track record of successful initiative management involving senior stakeholders.
  • Exceptional skills in executive communication, facilitation, and stakeholder management.

Responsibilities

  • Lead cross-functional pharmaceutical development programs through all lifecycle stages.
  • Develop and maintain project plans aligned with business objectives and regulatory requirements.
  • Oversee regulatory submission and quality system improvement initiatives.
  • Create integrated launch readiness plans across various functions.
  • Facilitate assessments and tracking of launch readiness milestones.
  • Support market access, pricing, and patient services initiatives.

Benefits

  • 100% employer-paid health coverage.
  • 401(k) matching program.
  • Business development incentives.
  • Performance bonuses.
  • Flexible hybrid work environment with a minimum of three days in-office.
Full Job Description
Description

Position Summary

IPM is seeking experienced professionals to lead complex pharmaceutical projects across the product lifecycle-from development and regulatory execution through commercialization, launch readiness, and post-launch management. The ideal candidate combines strong project and program leadership with hands-on product lifecycle leadership experience and can successfully operate across a wide range of client environments.

This role is designed for professionals who can lead development-focused initiatives while also bringing commercialization and launch-readiness experience. Successful consultants will build structure, drive accountability, manage risks, facilitate decision-making, and deliver executive-ready outputs that move critical programs forward.

Key Responsibilities

Lead Product Development & Lifecycle Programs
  • Lead cross-functional pharmaceutical development programs across pre-clinical, clinical, regulatory, CMC, quality, supply chain, commercialization, and post-approval stages
  • Develop and maintain integrated project plans aligned to business objectives, critical milestones, and regulatory requirements

Support Regulatory, Quality & Operational Readiness Initiatives
  • Lead planning and execution for regulatory submission readiness, inspection readiness, quality system improvements, technology transfer, manufacturing scale-up, labeling, and supply initiatives.

Drive Commercialization & Launch Readiness
  • Develop integrated launch readiness plans spanning Commercial, Medical Affairs, Market Access, Regulatory, Supply Chain, Patient Services, and Analytics functions.
  • Facilitate launch readiness assessments, governance reviews, milestone tracking, and post-launch stabilization planning.
  • Support initiatives involving market access, pricing and contracting, reimbursement, HEOR/RWE, patient access, specialty pharmacy, field readiness, and commercial operations.

Required Qualifications
  • 8-15+ years of experience within the pharmaceutical industry leading: product development lifecycle projects, regulatory, quality and operational readiness initiatives, and commercialization and launch readiness projects
  • Minimum 3 years of project or program management experience or equivalent cross-functional leadership responsibility
  • Demonstrated success leading complex initiatives involving senior stakeholders.
  • Excellent executive communication, facilitation, documentation, and stakeholder-management skills

Comprehensive compensation and benefits program: including 100% employer-paid health, 401(k) matching, business development incentives, and performance bonus amongst many other elements. Salary Range: $125,000 - $180,000

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.

Disclaimer: Where a specific pay range is noted, it is a good faith estimate at the time of this posting. The actual salary offered will be based on experience, skills, qualifications, and market/business considerations.

IPM's hybrid work environment requires a minimum of three days in the office. The specific days are flexible and may vary depending on project schedules and meetings. On-site locations may also vary. In addition, we follow our clients' guidance on on-site requirements, so the minimum number of days in the office may increase depending on the client and project assignment.

About Integrated Project Management

Integrated Project Management Company, Inc. (IPM) is a project management consulting firm that provides project management services to clients in various industries, including healthcare, life sciences, and consumer products. The company offers a range of services, including project management, process improvement, and organizational change management. IPM was founded in 1988 and is headquartered in Lisle, Illinois.
Learn more about Integrated Project Management
Size
500 employees
Industry
Founded
1988

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