Spyre Therapeutics

Executive Director, Program Management

Spyre Therapeutics

full-time

Posted on:

Location Type: Remote

Location: United States

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Salary

💰 $295,000 - $313,000 per year

Job Level

Lead

About the role

  • 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

Requirements

  • 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.
Benefits
  • 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
  • Commitment to provide professional development opportunities.
  • Remote working environment with frequent in-person meetings to address complex problems and build relationships.

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard skills
program managementproject documentationrisk managementGantt chartsreport generationclinical developmentdrug development processregulatory requirementsmonoclonal antibody therapeuticsplanning
Soft skills
critical thinkingattention to detailfacilitationcommunicationleadershipinterpersonal skillsadaptabilityorganizationcollaborationproblem-solving