Director, Program Management

Kiniksa Pharmaceuticals • Lexington, MA

30d • $230,000 - $242,000 • Onsite

About The Position

Kiniksa Pharmaceuticals is a commercial‑stage biopharmaceutical company developing and commercializing novel therapies for diseases with unmet need, with a focus on cardiovascular indications. With deep expertise in immunology and inflammation, Kiniksa is advancing a growing portfolio of approved and investigational medicines, anchored by its lead product, ARCALYST®, the first and only FDA‑approved therapy for recurrent pericarditis. Grounded in rigorous science and bold innovation, the company fosters a highly collaborative, patient‑first culture led by accomplished life sciences leaders. At Kiniksa, talented individuals are trusted and empowered to make a real impact—shaping the future of medicine while improving the lives of patients who need it most.
We are seeking an energetic and motivated individual who seeks to lead from the front and is driven to make a lasting impact. The Director, Program Management, is responsible for providing hands-on leadership and support for high priority development programs within Kiniksa’s global biopharmaceutical pipeline. Serving as an operational backbone for programs, this role will translate program strategy and plans into operational execution while driving the delivery of development milestones in alignment with corporate and program goals.
This is an excellent opportunity for candidates who work with a sense of urgency, enjoy distilling complexity into clarity, can effectively align inputs from different perspectives, and can think critically to synthesize information from different perspectives. Emphasis will be on prior drug development experience, good communication skills (verbal, written and non-verbal), problem-solving skills, and an adaptable growth mindset.
The ideal candidate is a high impact leader with executive presence who can see the big picture while diving deep to execute effectively.

Requirements

• Bachelor’s degree in Life Sciences, Pharmacy or related discipline, advanced degree preferred (e.g., PhD, PharmD, MBA)
• At least 5 years of experience in the biopharma industry in a cross-functional project or program management role with a track record of managing clinical stage programs
• Understanding of the drug development process, including advancing product candidates from IND/CTA submission to late-stage development and ultimately registration with health authorities
• Strong analytical and problem-solving skills with keen attention to detail and an unrelenting drive to deliver results in a fast-paced and dynamic environment
• Ability to thrive in a matrixed, cross-functional team setting while cultivating positive, constructive working relationships across the organization
• Proficiency in using standard project management software (e.g., Smartsheet) and the Microsoft Office suite (i.e., PowerPoint, Word, Excel, SharePoint, etc.)

Nice To Haves

• Proven leadership in cross-functional program management, driving integrated development plans and delivering key milestones across clinical, regulatory, CMC, and commercial functions
• Strong ability to translate complex strategy into operational execution, ensuring alignment, clarity, and accountability across matrixed teams in fast-paced environments
• Expertise in risk management and scenario planning, proactively identifying challenges and implementing data-driven mitigation strategies to keep programs on track
• Effective communicator with executive presence, skilled in stakeholder alignment, performance tracking, and driving decision-making through clear insights, dashboards, and program governance

Responsibilities

• Develop program plans and drive execution: partner with functional leaders and key stakeholders to create the Integrated Development Plan, define critical path activities and program milestones, ensure cross-functional team awareness and readiness to execute on key activities, and drive day-to-day execution of the IDP.
• Deliver on key program milestones: collaborate with functional team leads across clinical operations, clinical development, regulatory, CMC, nonclinical, finance, commercial, medical affairs, and quality assurance, to deliver on program milestones (e.g., regulatory submissions, health authority meetings, clinical trial enrollment targets, data readouts), and ensure continued alignment.
• Manage cross-functional team meetings: work with team members to develop meeting agendas, ensure stakeholder preparedness for meetings, capture and distribute minutes, and ensure follow-through on action items.
• Risk management and scenario planning: proactively identify potential program risks and challenges, work with team members to define relevant mitigation strategies, prepare data-driven scenarios to enable decision making (team level and/or senior level).
• Monitor and communicate progress: maintain clear and accurate program, dashboards for tracking program goals and key metrics to monitor and assess program performance.
• Support budget processes: Partner with finance team and functional leads to develop and refine program assumptions for budget purposes throughout forecasting cycles.
• Enhance Program Management best practices – Collaborate across the Program Management team and broader organization to establish and champion best practices.

Benefits

• Kiniksa is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, transgender status, age, genetics, national origin, protected veteran status, or disability status, or any other legally protected category. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

What This Job Offers

• Job Type: Full-time
• Career Level: Director