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Software Engineering/Development: Technical Project Manager - Clinical Systems Parsippany, NJ, [...]
- New York, New York, United States
- New York, New York, United States
À propos
Job Description:
Work closely with information systems, software development, testing, product, and business stakeholders to gather requirements, define scope, and align priorities/deliverables ensuring smooth transitions between teams
Own end-to-end delivery of larger platform features and enhancements, breaking down ambiguous requests into actionable, trackable work
Translate business and clinical needs into clear, testable requirements and maintain supporting documentation to ensure alignment across teams
Organize and manage backlogs in Jira, implement lightweight sprint structures where appropriate, and create visibility into active work, risks, and timelines
Help transition toward more structured, milestone‑driven releases, including quarterly planning and progress tracking
Work closely with development and DevOps to understand Git‑based workflows, branching strategies, environments, and deployment processes
Establish clear deliverables, milestones, and flagging risks early, proposing solutions when applicable, while maintaining strong working relationships
Ensure requirements and deliverables are defined clearly enough to support testing, validation, and regulatory expectations
Core Requirements:
Bachelor’s degree in computer science, information technology, or a related field (or equivalent experience)
5–10 years of experience in technical project management, product delivery, or similar roles
Experience delivering web‑based platforms or complex software systems
Strong understanding of software development workflows, including Git‑based version control, branching, environments, and release processes
Demonstrated experience using tools such as Jira (or similar) to manage backlogs, sprints, and delivery tracking
Working knowledge of Agile/Scrum methodologies with the ability to apply them pragmatically
Proven ability to work projects, even those with loosely defined concepts, through completion
Familiarity with validation processes or FDA‑related workflows and experience in clinical systems, medical imaging, or regulated environments
Photography or imaging domain knowledge, or experience working with image‑based systems
Project management certifications (PMP, CSPO, or similar)
Canfield Scientific, Inc. is a core imaging lab providing custom photographic systems, image monitoring, and centralized analysis services for the pharmaceutical, biotechnology and cosmetics industries supporting global clinical trials providing primary endpoint data and supporting documentation. Canfield offers comprehensive benefits to its eligible full‑time employees. These include paid days off, medical, dental, and vision insurance, may be eligible for a discretionary bonus, and a 401(k) plan with employer match (currently set at 50%). The anticipated salary range for the position is $110,000 - $120,000 annually. This is dependent upon consideration of multiple factors when determining a base salary such as a candidate’s experience, education, and current market conditions. If the role is eligible for full benefits, it will be discussed with you during the interview process. Canfield’s imaging equipment leads the industry providing high‑quality, registered, reproducible clinical images. This, together with proactive clinical image monitoring and a world class quality assurance regimen, sets the gold standard in image quality for clinical studies.
Apply Here Please submit resumes with cover letter to jobs@canfieldsci.com or click below for immediate consideration. Please include the position title in the subject line.
We are proud to be an equal opportunity employer.
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Compétences linguistiques
- English
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