Software Engineering​/Development: Clinical Outcome Technical Project Manager

Software Engineering/Development:
Clinical Outcome Technical Project Manager

Apply for the Software Engineering/Development:
Clinical Outcome Technical Project Manager role at Canfield Scientific
.

The ideal candidate has strong communication skills, is self‑motivated and passionate, and possesses excellent time‑management skills. This role ensures that digital platforms for patient‑reported outcomes (PROs), electronic clinical outcome assessments (eCOA), and other trial technologies are deployed effectively, compliant with regulatory standards, and aligned with study protocols. The candidate will have deep expertise in clinical research operations, regulatory frameworks, and digital health technologies used in drug and device development.

• Manage the design, configuration, and deployment of in‑house eCOA and PRO systems across global clinical trials
• Collaborate with clinical operations, data management, biostatistics, and regulatory affairs to ensure technology solutions meet protocol requirements
• Develop mockups, write software requirements, and interface directly with development teams
• Communicate status, issues, barriers, metrics, reports, and any other required information to stakeholders in a timely manner
• Work effectively in a changing, high‑impact, fast‑paced environment with challenging deadlines and resource constraints, managing multiple projects with tight deadlines
• Create documentation for the project and/or individual aspects of the project as needed
• Support postmortem reviews and improvement initiatives

• Bachelor’s degree or equivalent education and/or experience
• At least 3 years’ related experience in system development, lifecycle methodology, and other disciplines relevant to eCOA system design, such as statistics, economics and validation of clinical data gathering instruments
• Strong knowledge of clinical outcome assessments (COAs), eCOA platforms, and digital health technologies
• Familiarity with regulatory requirements for clinical trials and patient data
• Proficiency in Microsoft operating systems
• Strong written and verbal communication skills

• Knowledgeable of the software development life cycle
• PMP Certification

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. Canfield offers comprehensive benefits to its eligible full‑time employees, including paid days off, medical, dental, and vision insurance, discretionary bonus eligibility, and a 401(k) plan with a 50% employer match.

$85,000 – $100,000 annually, dependent upon experience, education, and market conditions.