Director Program Management

We are seeking a proactive and committed Director, Program Management to provide strategic leadership and operational excellence for TUB-040, Tubulis’ lead program, as well as for our portfolio of innovative therapeutic programs spanning early- and late-stage clinical development.

The Director will partner closely with leaders in Clinical Development, Regulatory, CMC, Biomarkers, PK, Nonclinical, Commercial, and other functions to ensure timely delivery of key milestones, robust risk management, and smooth progression of programs toward regulatory approval and commercialization.

Key Responsibilities

• Lead the cross-functional TUB-040 program team through all stages of clinical development — from IND-enabling studies to pivotal trials and regulatory submissions.
• Serve as the primary point of contact for program strategy, planning, execution, and milestone delivery.
• Develop and maintain integrated program plans, budgets, timelines, and risk management strategies aligned with corporate objectives.
• Partner with functional leaders (Clinical Development, Clinical Operations, Regulatory, CMC, Biostatistics, Biomarkers, Commercial, etc.) to ensure requirements are well-defined, resourced, and executed with quality.
• Drive effective decision‑making by preparing clear program updates and recommendations for governance committees.
• Provide mentorship within the Program Management function, fostering process improvements and building organizational capabilities.
• Encourage collaboration, guide team members, address challenges, and promote a positive working environment.
• Maintain open communication with the VP Program Management, team members, partners, and key stakeholders.

Candidate Profile

• Bachelor’s or advanced degree in a relevant scientific discipline.
• 10+ years of experience in the biotechnology or pharmaceutical industry, with significant program/project management leadership.
• Demonstrated success advancing programs through multiple phases of clinical development (IND/CTA, Phase I–III, BLA/MAA, launch, lifecycle management).
• Proven expertise in late‑stage development and pivotal trials.
• Comprehensive knowledge of clinical development, regulatory requirements, GxP, CMC, nonclinical, and commercialization aspects.
• Strong leadership, organizational, and interpersonal skills with the ability to inspire and motivate cross‑functional teams.
• Excellent communication and presentation skills; able to synthesize complex data and present compelling updates to leadership and stakeholders.
• Proficiency with project management tools (MS Project, Excel, PowerPoint, Think‑Cell).
• Self‑starter with strong problem‑solving skills; comfortable working in a fast‑paced, dynamic environment.

Why us?

At Tubulis, curiosity and innovation drive us to transform cancer treatment. We are a fast‑growing biotech where science meets passion—and where you have the chance to grow with us.

• Impact that matters : Contribute to breakthrough therapies.
• Global mindset : Work in an international, diverse team.
• Grow & thrive : Develop your career in a supportive, fast‑moving environment.
• Innovation every day : Push boundaries with cutting‑edge science.

At Tubulis, your ideas matter, your growth matters—and together, we make a difference.

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