200+ applicants

Company

Original Job Post

enGene · 2 days ago

Vice President, Program Management

Waltham, MA

Full-time

Remote

Executive

5+ years exp

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Responsibilities

Lead program management activities for enGene’s EG-70 product candidate across all clinical programs, including registration for lead indication of BCG-unresponsive NMIBC with Cis

Guide the cross-functional product team through late-stage clinical development by collaborating to execute an integrated development plan through registration

Work with technical operations/CMC, clinical operations, regulatory, and commercial to ensure critical functional activities are fully integrated into the product development plan

Achieve organizational alignment and seamless execution by working cross functionally within enGene and with selected CROs. Develop strong working relationships with key external stakeholders

Define critical path, at-risk activities, and inter-dependencies. Anticipate bottlenecks, and clear barriers to progress program level scenario planning and risk management

Identify, track, and support resolution efforts for all program-related issues

Relay deviations from program plans to the program team and management

Coordinate and lead regulatory project-team meetings. Facilitate clear presentation of action items and critical path deliverables, calling for and driving action if required

Serve as liaison to C-suite and executive leadership team for program-level topics

Track program progress against the plan, working with department heads to identify and resolve resource constraints consistent with corporate priorities

Support active portfolio management (budget, resources, stage-gates where relevant) and decision making; monitor progress of portfolio/program strategy, goals, and metrics

Ensure uniformity between programs including agendas, meeting minutes, and other program documentation.

Preparation of materials for C-suite and BoD as needed

Qualification

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Program ManagementCMCPortfolio ManagementStrategic PlanningRisk ManagementRisk AnalysisDecision AnalysisContingency PlanningBudget ManagementProblem-SolvingCommunicationNegotiationAdaptabilityPrioritizationDecision Making

Required

Bachelor's degree in science or related field and an advanced degree MS/PhD preferred

At least 10 years of relevant biotech or pharmaceutical industry experience with 5-7+ years in program management. Deep functional experience in CMC, commercialization, or late-stage regulatory preferred

Hands-on experience in leading program management activities for global oncology or urology programs in early and late stages of clinical development, ideally through registration

Oncology or urology experience required

Portfolio management/strategic Planning/risk management experience required, with experience in risk analysis, decision analysis, and contingency planning

Strong facilitation, negotiation, and dynamic communication skills across various functions and levels of governance

Excellent written and verbal communication. Must be able to clearly and concisely communicate complex program information in both formal and informal settings, both verbally and in presentation media

Experience setting and maintaining budgets

Able to handle complexity and ambiguity as well as be able to prioritize effectively