Consultant, Pharmaceutical Development and Commercialization
$115,000–$140,000 year
HybridChicago, Illinois, United States
Job Summary
Lead cross-functional pharmaceutical development programs across pre-clinical, clinical, regulatory, CMC, quality, supply chain, commercialization, and post-approval stages. Develop integrated project plans aligned to business objectives, critical milestones, and regulatory requirements. Lead planning and execution for regulatory submission readiness, inspection readiness, quality system improvements, technology transfer, manufacturing scale-up, labeling, and supply initiatives. 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. This role requires 8–15+ years of experience within the pharmaceutical industry leading product development lifecycle, regulatory, quality, and commercialization projects, with a minimum of 3 years in project or program management. Salary range is $115,000 - $140,000. Applicants must be authorized to work in the U.S. IPM partners with pharmaceutical, biotechnology, and medical technology organizations to lead strategic portfolios across product development, regulatory affairs, quality, and operational transformation.
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
- Applicants must be authorized to work for any employer in the U.S.
- 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
- 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
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