Role Summary

The Senior Director of Program Management will play a crucial role in the planning and execution of our development programs. This position requires a proactive individual who thrives in a dynamic, rapidly growing startup environment.

Key Responsibilities

• Meticulously maintain and track detailed integrated program timelines ensuring alignment across functions on dependencies and assumptions crucial for corporate goals. Recognize and alert stakeholders when projects are on or near critical paths to key milestones. Communicate progress transparently and address issues promptly.
• Manage cross-functional meetings efficiently, ensuring clear objectives, documenting outcomes, information, and action items, and following up on tasks with team members.
• Develop and upkeep project documentation including meeting materials, minutes, action item logs, decision trackers and dashboards.
• Proactively identify, monitor, communicate and propose mitigation options for program risks.
• Collaborate across functions including Pre-clinical, Clinical Development, Technical Operations, Regulatory, Quality, Finance and Legal to ensure alignment.
• Play a pivotal role within the Portfolio Management and Operations team, providing guidance on best practices, developing team resources, tools and templates, and nurturing a culture of excellence, innovation, and accountability.
• Other duties as assigned.

Ideal Candidate

• Demonstrated proficiency in overseeing complex development programs, guiding them from Investigational new Drug IND) stage through Phase 2 clinical development, with a strong preference for monoclonal antibody therapeutics experience.
• Bachelor’s degree in a science-related field required; an advanced degree is preferred.
• Minimum of 10 years of relevant experience in biotechnology or pharmaceuticals, with at least 5 years directly in program management.
• Strong planning skills, critical thinking abilities and keen attention to detail.
• Ability to juggle multiple tasks, adapt to shifting priorities in a fast-paced environment.
• Excellent facilitation, communication, and leadership skills.
• Strong interpersonal skills and the ability to interact well with all employee levels.
• Expert in creating Gantt charts in Smartsheet, Think-Cell and Office Timeline Pro software, along with report generation.
• In-depth understanding of the drug development process, regulatory requirements, and industry standards.
• Willingness to travel up to 10% annually, including quarterly all hands meetings and ad hoc development team gatherings.

What We Offer

• Opportunity to work in a fast-paced, highly dynamic environment where you help shape the culture of our young company, wear multiple hats, and learn quickly.
• Market-competitive compensation and benefits package, including base salary, performance bonus, equity grant opportunities, health, welfare & retirement benefits.
• Unlimited PTO
• Two, one-week company-wide shutdowns each year.
• Commitment to growing you professionally and providing access to resources to further your development.
• 100% remote team with frequent in-person meetings to build relationships and problem solve.

The expected salary range offer for this role is $255,000 to $284,000. Actual pay offered may vary depending on job related knowledge, experience, education, and geographic location.