Lead Technical Systems Analyst

Foundation Medicine; Boston (MA); Sur place; USD 120 000 - 180 000; Plein temps

Résumé du poste

Foundation Medicine seeks a Lead Technical Systems Analyst to translate complex business needs into scalable technical specifications across multiple enterprise platforms, guiding architectural decisions and promoting best practices in analysis and delivery.

You will manage dependencies, mentor analysts and engineers, and produce executive decision materials to drive seamless software delivery in regulated bioinformatics workflows.

Qualifications

• Bachelor's degree in life sciences, business, or technology required.
• 8+ years in technical analysis, product ownership, or related roles, with experience leading multi-stream enterprise initiatives.

Responsabilités

• Decompose initiatives.
• Evaluate architectural approaches.
• Manage cross-team dependencies.
• Establish analysis standards.
• Produce executive decision materials.
• Mentor analysts and engineers.

Connaissances

Stakeholder management

Requirements gathering

Formation

Bachelor's degree in life sciences, business, or technology

Outils

Jira

Confluence

Description du poste

Role

Lead Technical Systems Analyst responsible for translating complex business needs into scalable technical specifications across multiple enterprise platforms, guiding architectural decisions, and promoting best practices in analysis and delivery.

Objectives

Ensure seamless software delivery, manage dependencies and risks, and foster a culture of technical rigor and continuous improvement.

Responsibilities

• Decompose initiatives
• Evaluate architectural approaches
• Manage cross-team dependencies
• Establish analysis standards
• Produce executive decision materials
• Mentor analysts and engineers

Requirements

• Bachelor's in life sciences, business, or technology;
• 8+ years in technical analysis, product ownership, or related roles, with experience leading multi-stream enterprise initiatives.

Preferred

• 5+ years in life sciences
• Familiarity with regulated environments (IEC 62304, FDA 21 CFR Part 11, GDPR)
• Proficiency with tools like Jira and Confluence
• Agile certifications (e.g., CSPO)
• Strong stakeholder management skills.

High Value

• Experience in regulated software development within biopharma, especially in quality, clinical laboratory, or genomics workflows;
• Working knowledge of HIPAA and patient data privacy.

Work Setup

Unspecified; no travel indicated.