Associate Director, Technical Product Management (AI)

Location: Hybrid; primary location: North Wales, Pennsylvania, USA. Available to residents of the United States, Canada, and Puerto Rico.

Salary: $142,400–$224,100 annually for the primary location; eligible for annual bonus and long-term incentive, if applicable.

Company

hirify.global develops science-based healthcare solutions and life-changing therapies, with an Information Technology organization focused on digital innovation and AI adoption.

What you will do

• Develop and implement Planning and Workflow strategies supporting Clinical Operations, Regulatory, Medical Affairs, and related business requirements while ensuring quality and compliance.
• Translate business problems and stakeholder input into actionable, strategically aligned product backlogs.
• Lead continuous discovery through user research, interviews, surveys, usability testing, and business-case development.
• Define product vision, principles, strategy, and measurable outcomes; prioritize delivery with the product team.
• Partner with engineers, architects, business owners, UX, and other stakeholders to deliver high-quality features through Agile methodologies, automated testing, and Digital SDLC.
• Resolve cross-team delivery dependencies, track AI adoption and value metrics, manage TCO and vendor negotiations, and lead performance and career development for IT team members.

Requirements

• Bachelor’s degree in Computer Science, Engineering, Information Systems, Life Science, or a related field.
• 8+ years of relevant IT or pharmaceutical experience, including 3+ years of Product Management experience using Agile methodologies and leadership experience.
• Passion for using AI to improve productivity and solve problems.
• Product mindset covering discovery, user experience, and engineering execution.
• Demonstrated leadership and people-management skills, including setting direction, motivating team members, performance management, career development, goal setting, and feedback.
• Excellent communication and interpersonal skills, with the ability to build trust across cross-functional teams in a global environment.
• Self-motivated, curious, collaborative, and able to foster an inclusive culture.

Nice to have

• Experience in a regulated industry such as pharmaceuticals or biotechnology, especially Clinical Operations, Regulatory, Medical Affairs, Planning and Supply Chain, Discovery, or Research.
• Experience building and supporting large-scale IT solutions with modern technologies, including work in a GxP environment and familiarity with 21 CFR Part 11 and ICH-GCP guidelines.
• Experience defining, measuring, and reporting success metrics.
• Knowledge of cloud data lakes or lakehouses, data integrations, automation, Veeva Workbench, or master data management.

Culture & Benefits

• Collaborative, inclusive global environment with cross-functional work across IT and business stakeholders.
• Hybrid work arrangement.
• Medical, dental, vision, and other insurance benefits for employees and families.
• Retirement benefits including 401(k), paid holidays, vacation, compassionate leave, and sick days.
• Annual bonus and long-term incentive eligibility where applicable.