Director – Early Stage Program Development

in Healthcare + Life Sciences
  • Waltham, Massachusetts View on Map
  • Salary: $210,000.00 - $240,000.00
Permanent

Job Detail

  • Experience Level Director
  • Degree Type Master of Science (MS)
  • Employment Full Time
  • Working Type Hybrid
  • Job Reference 0000018008
  • Salary Type Annually
  • Industry Pharmaceuticals
  • Selling Points

    Drive transformative early-stage program development in a leading biopharmaceutical environment. Collaborate across disciplines to advance innovation and scientific progress. Hybrid work model ensures flexibility and collaborative engagement.

Job Description

Overview

  • Lead strategic program management for early-stage initiatives in a dynamic biopharmaceutical environment, driving innovation and scientific advancement.
  • Collaborate with cross-functional teams to align research, translational science, and development strategies for impactful outcomes.
  • Ensure integrated planning and execution, maintaining alignment with corporate objectives and regulatory requirements.
  • Support scientific program progression through effective risk management and proactive issue resolution.
  • Contribute to scenario planning, governance materials, and strategic communications for organizational leadership.
  • Enhance program management processes to support complex, science-driven initiatives and foster innovation.
  • Provide leadership in matrixed environments, encouraging collaboration across diverse teams and disciplines.
  • Hybrid work model offering flexibility and on-site engagement for optimal productivity.

Key Responsibilities & Duties

  • Develop and execute cross-functional scientific program plans, emphasizing research strategy and translational integration.
  • Facilitate alignment of discovery, preclinical, translational, and clinical insights into cohesive strategies.
  • Identify and address gaps and interdependencies across research and development functions.
  • Ensure scientific priorities align with broader development, regulatory, and corporate objectives.
  • Track progress against milestones, manage risks, and escalate issues as needed to ensure program success.
  • Lead core and sub-team meetings, translating scientific strategies into actionable plans.
  • Support development and maintenance of timelines, budgets, and planning tools for efficient program execution.
  • Contribute to lifecycle strategy and regulatory submission planning, ensuring compliance and readiness.

Job Requirements

  • Master’s degree in a scientific discipline; PhD preferred for advanced expertise.
  • 12+ years of biopharmaceutical industry experience, including program management and drug development.
  • Hands-on experience in research, translational science, or preclinical development is essential.
  • Expertise in neuroscience, CNS, or translational medicine is highly desirable.
  • Proficiency in MS Project, MS Excel; familiarity with Planview and SmartSheet is advantageous.
  • Exceptional communication skills and ability to manage time effectively in dynamic settings.
  • Experience transitioning programs from early/mid-stage to later-stage development successfully.
  • Strong organizational instincts and ability to operate effectively in matrixed environments.
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