Consultant, Pharmaceutical Development and Commercialization
$115,000–$140,000 year
HybridIllinois, 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, and manufacturing scale-up. 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, reimbursement, HEOR/RWE, patient access, specialty pharmacy, and field readiness. This role requires 8–15+ years of industry experience and 3+ years in project management. Salary range is $115,000 - $140,000.
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
- 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
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