Director, Program Management I & I Full Life Cycle
Monte Rosa Therapeutics · Boston, MA · 2 mo ago
Project ManagementFull-time
About the role
The Associate Director of Program Management will serve as a strategic and operational leader for priority immunology and inflammation programs, driving assets from mid- to late-stage development through regulatory submission. This role is designed for a hands-on, agile leader who thrives in a fast-paced biotechnology environment and can rapidly translate evolving science into executable development strategy.
Responsibilities
- Serve as a strategic and operational lead for one or more immunology/inflammation programs, ensuring alignment between clinical strategy, translational insights, and regulatory pathways.
- Develop and maintain integrated, cross-functional development plans across clinical, regulatory, CMC, manufacturing, and translational functions.
- Lead scenario planning exercises to evaluate alternative development pathways, indication sequencing, acceleration opportunities, and capital-efficient trade-offs.
- Continuously pressure-test timelines and critical paths, proactively identifying opportunities to streamline execution without compromising quality.
- Establish proactive risk identification and mitigation frameworks tailored to immunology/inflammation programs, including biomarker risk, patient heterogeneity, regulatory complexity, and competitive landscape shifts.
- Lead high-quality risk discussions at the Global Program Team level with timely escalation of high-impact issues.
- Develop contingency strategies for clinical, manufacturing, or regulatory inflection points.
- Maintain program-level budget and resource health in alignment with corporate priorities.
- Ensure clarity of functional accountabilities and decision rights in a lean, matrixed biotech structure.
- Partner with functional leaders during long-range planning and portfolio prioritization exercises.
- Build and maintain practical, real-time tracking tools (e.g., Smartsheet dashboards, integrated timelines, risk logs) that enable rapid visibility and decision-making.
- Prepare concise, executive-ready materials that distill complex scientific and operational issues into clear recommendations.
- Lead continuous improvement initiatives within Program Management to enhance agility, transparency, and execution discipline.
Requirements
- 12+ years of experience in biotechnology or pharmaceutical drug development.
- Minimum 8 years of program/project management experience leading cross-functional development teams.
- Demonstrated experience advancing immunology and/or inflammation assets through Phase 2 and Phase 3 development.
- Experience preparing for and supporting major regulatory interactions (e.g., End-of-Phase 2 meetings, NDA/BLA submissions).
- Experience operating in small-to-mid-sized biotech environments where agility and hands-on leadership are required.
Qualifications
- BS required; advanced degree (MS, PhD, or MBA) strongly preferred.
- PMP certification desirable but not required.
Skills
- Strong understanding of immunology and inflammation biology, clinical endpoints, biomarker strategy, and regulatory considerations.
- Deep knowledge of end-to-end drug development within a resource-conscious biotech setting.
- Demonstrated ability to lead through ambiguity and adapt strategy as data emerge.
- Proven success influencing senior stakeholders in a highly matrixed environment.
- Expertise in integrated planning, risk management, and scenario modeling.
- Strong executive presence with the ability to communicate complex scientific and operational topics clearly and concisely.
- Proficiency with modern project management and collaboration tools (e.g., Smartsheet, MS Project, Teams).
- Exceptional organizational skills with the ability to manage multiple interdependent workstreams simultaneously.
- High emotional intelligence, strong conflict resolution skills, and the ability to build trust across scientific and operational teams.
- Comfort operating with urgency, limited infrastructure, and evolving priorities typical of innovative biotech companies.
Benefits
N/A
Pay
N/A
Schedule
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