Project Manager

Drug Development PM

Location: Onsite 2-3 days/week in Princeton Pike, NJ

Overview

Our client is in immediate need of a Program Manager to serve as a strategic partner to the Global Program Lead (GPL), driving cross-functional planning, execution, and risk management across one or more development assets and indications. This consultant will be responsible for developing and maintaining integrated development plans, ensuring alignment across functional teams, and helping guide programs from early clinical development through commercialization.

Responsibiliti

• esPartner with the Global Program Lead (GPL) to develop and execute integrated development strategies and target product profile
• s.Lead cross-functional planning and execution across clinical, regulatory, CMC, nonclinical, and commercial function
• s.Develop and maintain integrated project timelines, scenario plans, and risk mitigation strategie
• s.Facilitate governance, decision-making, and team alignment to ensure achievement of key program milestone
• s.Lead program-level risk management activities and ensure timely escalation of critical risk
• s.Monitor program budget and resource requirements and support annual planning processe
• s.Drive cross-functional communication and stakeholder management across global team
• s.Present program updates, recommendations, and strategic considerations to senior leadership and governance committee

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Qualificat

• ionsAdvanced degree preferred (MBA, MS, PhD); PMP certification is a p
• lus.10 years of drug development program/project management experie
• nce.Experience supporting programs from early clinical development through commercializat
• ion.Strong understanding of global drug development processes, including regulatory submissions and lifecycle managem
• ent.Demonstrated success leading highly visible, cross-functional development progr
• ams.Proven matrix leadership experience with the ability to influence stakeholders without direct author
• ity.Strong expertise in program planning, risk management, resource planning, and stakeholder managem
• ent.Excellent communication, presentation, and executive-facing ski

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Preferred Qualific

• ationsNeuroscience drug development exper
• ience.Experience supporting global regulatory submissions (IND, CTA, NDA, BLA, MAA,
• etc.).Advanced degree (MBA, MS, or
• PhD).PMP certific

ati