Technical Product Manager

Posted 51ds ago

Employment Information

Education
Salary
Experience
Job Type

Report this job

Job expired or something wrong with this job?

Job Description

Technical Product Manager leading product development for clinical trial solutions that improve patient outcomes. Collaborating with technical teams and stakeholders to drive innovative, data‑driven products.

Responsibilities:

  • Align product roadmaps with overall vision in partnership with Product Line Leaders and Upstream Product Managers
  • Monitor emerging technologies and industry trends to inform strategy
  • Develop and maintain multi‑year release plans and initiatives
  • Collaborate with technical teams on architecture, UX, and key capabilities
  • Lead business architecture and workflows for assigned product areas
  • Validate concepts and requirements through stakeholder feedback
  • Balance priorities across architecture, maintenance, and new features
  • Support agile ceremonies and team retrospectives
  • Partner with Product Owners to ensure accurate knowledge transfer
  • Act as subject matter expert in cross‑functional initiatives
  • Contribute to internal knowledge bases and user documentation
  • Lead release readiness and commercial launch activities
  • May manage individual contributors

Requirements:

  • Bachelor’s degree in business, science, technology, or medicine (Master’s in Business Administration preferred)
  • 3+ years of product management experience, ideally in healthcare or clinical trials
  • Strong technical acumen and ability to communicate across teams
  • Experience across the full product lifecycle and solid domain knowledge in life sciences
  • Proven collaboration with UX/UI teams on business and data workflows
  • Excellent prioritization and decision‑making in agile environments
  • Strong customer engagement and communication skills
  • Leadership experience with the ability to influence across levels
  • Experience developing specifications within a Quality Management System
  • Familiarity with FDA 510(k), CE Marking, and global device approvals
  • Understanding of GCP, 21 CFR Part 11, device security, GMP, MDD, MDR

Benefits:

  • Competitive compensation
  • Flexible work schedules
  • Attractive PTO plan
  • Engaging employee programs