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.
Director – Early Stage Program Development
in Healthcare + Life Sciences PermanentJob Detail
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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