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[Remote] Sr. Director, Program Management

Remote · Egypt Full-time

Note: The job is a remote job and is open to candidates in USA. Nektar Therapeutics is seeking a Senior Director of Program Management to lead development-side program planning and execution from late clinical development through BLA submission. This role involves partnering with various stakeholders to ensure integrated plans and disciplined execution are in place for timely and high-quality submissions.

Responsibilities

  • Lead integrated program management for indication-specific portfolio, with primary accountability for pre-BLA execution, submission readiness, and delivery of key development milestones
  • Build and maintain integrated development plans, including critical-path timelines, governance cadence, decision logs, and risk and dependency management across Clinical, Regulatory, CMC, Safety, Quality, Clinical Operations, Biometrics, Medical Affairs, and Commercial
  • Translate portfolio strategy into clear objectives, milestones, resourcing assumptions, and executable cross-functional workplans in partnership with development leadership
  • Drive BLA-readiness planning, including coordination of submission workstreams, cross-functional deliverables, scenario planning, issue resolution, and executive-level progress reporting
  • Lead program governance, ensuring clear decision framing, aligned agendas, disciplined action tracking, and timely escalation of risks, trade-offs, interdependencies, and external factors influencing development strategy
  • Integrate competitive intelligence benchmarking into program planning and governance by synthesizing relevant external development and regulatory insights to inform scenario planning, risk assessment, and leadership recommendations
  • Lead cross-functional problem solving in complex or fast-moving environments, ensuring clarity of priorities, accountabilities, timelines, and decision rights
  • Deliver portfolio-level communications, dashboards, and reporting to provide leadership visibility, enable informed decision making, and support disciplined execution
  • Coach and mentor program management team members and strengthen program management practices, tools, and operating rhythms across the portfolio
  • Drive continuous improvement in development operations, including use of AI-enabled tools and Smartsheet to enhance planning, reporting, automation, and knowledge management

Skills

  • Bachelor's degree in a scientific, healthcare, business, or related discipline required
  • Typically requires 15+ years of relevant pharmaceutical, biotechnology, or life sciences experience, including significant experience leading cross-functional drug development programs
  • Late-stage development and regulatory submission experience required
  • Deep understanding of global drug development and FDA regulatory processes, with direct experience supporting late-stage development and regulatory submissions
  • Demonstrated success leading complex, cross-functional pharmaceutical or biotechnology programs in matrixed environments
  • Executive presence and communication skills, with ability to synthesize complex information into clear, decision-ready recommendations
  • Proven ability to manage program risks, dependencies, budgets, external partners, and competing priorities while maintaining delivery discipline
  • Excellent analytical, planning, facilitation, and problem-solving skills
  • Proficiency with Microsoft Office and modern project/portfolio management tools
  • BLA experience strongly preferred
  • Experience synthesizing competitive intelligence, clinical/regulatory benchmarking, or external landscape insights to inform development plans, scenario analyses, and executive decision making preferred
  • Hands-on experience using AI-enabled productivity tools and Smartsheet for project planning, dashboards, workflow automation, risk tracking, and portfolio reporting
  • Experience in immunology, inflammatory diseases, dermatology, or atopic dermatitis preferred
  • Advanced degree preferred
  • PMP or other relevant project/program management certification preferred
  • Prior leadership of program management staff, governance teams, or executive decision forums preferred

Benefits

  • Annual performance bonus in accordance with the terms of the applicable plan, depending in part on company and individual performance and at the Company’s discretion
  • Health Insurance (Medical/Dental/Vision)
  • Disability Insurance
  • Holiday Pay
  • Paid Time Off (PTO)
  • 401(k) Match
  • Employee Stock Purchase Plan
  • Wellness Programs
  • Parental Leave Benefits (in accordance with the terms of applicable plans)

Company Overview

  • Nektar Therapeutics develops therapeutics based on its advanced polymer conjugate chemistry technology platform. It was founded in 1990, and is headquartered in San Francisco, California, USA, with a workforce of 51-200 employees. Its website is http://www.nektar.com.
  • Company H1B Sponsorship

  • Nektar Therapeutics has a track record of offering H1B sponsorships, with 1 in 2026, 2 in 2025, 1 in 2024, 3 in 2023, 14 in 2022, 15 in 2021, 13 in 2020. Please note that this does not guarantee sponsorship for this specific role.
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