Global Program Director, R&D Operations

Tevapharm

Parsippany-Troy Hills (NJ)

On-site

USD 150,000 - 190,000

Full time

3 days ago
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Benefits offered by this job

Health Insurance
401(k) with employer match
Paid Time Off
Employee Stock Purchase Plan

Job summary

Teva in New Jersey seeks a Global Program Associate Director to act as the operational engine of cross-functional drug development teams, ensuring alignment and timely execution across R&D, commercial, and TGO. You will build detailed plans, track milestones and budgets, and prepare dashboards and governance reports to support decision making.

The role requires an advanced degree and 8+ years in the pharmaceutical industry, with PMP or equivalent experience preferred for complex multinational

Qualifications

  • Advanced degree (MSC or MBA) with 8+ years in pharmaceutical industry.
  • Expert project management skills.
  • Strong organisational and communication skills, bridging diverse cross-functional and geographically diverse teams.
  • Advanced knowledge in drug product development.

Responsibilities

  • Strategic partnering with GPTD and GPT members to translate program strategy into actionable global integrated Asset plans (IAPs).
  • Coordinate preparation for program stage gates (endorsement for moving through development phases) in collaboration with GPT and GPTD.
  • Manage cross-functional alignment, ensure program goals, timelines, KPIs, and milestones are met.
  • Develop & maintain accurate project plans and forecasts in enterprise planning systems (PLM).
  • Manage GPT meeting logistics, drive alignment, and communicate status to stakeholders.

Skills

Project management
Cross-functional collaboration
Communication
Drug product development knowledge

Education

MSC or MBA

Tools

PLM software

Job description

Teva in New Jersey seeks a Global Program Associate Director to act as the operational engine of cross-functional drug development teams, ensuring alignment and timely execution across R&D, commercial, and TGO. You will build detailed plans, track milestones and budgets, and prepare dashboards and governance reports to support decision making.

The role requires an advanced degree and 8+ years in the pharmaceutical industry, with PMP or equivalent experience preferred for complex multinational

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