Senior Project Manager

Location: Hybrid role based in Boston, Massachusetts, United States; compliance with FMI attendance policies is required.

Salary: $112,600–$140,800 per year; discretionary annual bonus may be available.

Company

hirify.global develops clinical products and supports biopharma partnerships, laboratory expansion, and regulated product initiatives.

What you will do

• Plan and execute biopharma clinical product development, laboratory expansion, and other business-critical projects from concept initiation through potential global commercialization.
• Lead projects through the full project management lifecycle, managing scope, schedule, budget, resources, risks, communications, deliverables, and change control.
• Coordinate cross-functional teams, secure resources, delegate work, guide decisions, and build ownership in a complex matrixed environment.
• Manage written and oral communications with internal stakeholders, FMI governance, executive teams, and external biopharma partners.
• Track project metrics, coordinate phase reviews, escalate critical decisions, and drive process and systems effectiveness.
• Maintain quality-system compliance and ensure adherence to company, federal, country, and regulatory requirements.

Requirements

• Bachelor’s degree.
• At least 5 years of experience in program or project management; 7+ years is preferred.
• Proficiency in scope, schedule, resource, risk, and general program/project management principles.
• Effective written, verbal, communication, and presentation skills, including communication with all organizational levels and external customers.
• Demonstrated negotiation and conflict management skills.
• Experience working independently, within deadlines and resource constraints, and in ambiguous or changing conditions.
• Working knowledge of FDA, ISO, CLIA, and CAP regulations, plus understanding of HIPAA and patient data privacy.
• Commitment to FMI’s values: Integrity, Courage, and Passion.

Nice to have

• Graduate degree or advanced project management certification such as PgMP or PMP.
• Experience leading international or distributed large-scale product development projects using project management and product design and development frameworks.
• Experience with intercultural teams, project management tools, FDA-regulated products, and coordinating program details across disciplines.
• Experience with Waterfall and Agile methodologies, managing scope, roles, responsibilities, specifications, timelines, and resources.

Culture & Benefits

• Hybrid work arrangement with attendance requirements.
• Benefits are available for the position.
• Annual discretionary bonus may be based on individual and company performance.
• Work involves cross-functional collaboration and external biopharma relationships in a complex, matrixed environment.