Canfield Scientific
Software Engineering/Development: Clinical Outcome Technical Project Manager
Canfield Scientific, Parsippany, New Jersey, United States
Software Engineering/Development: Clinical Outcome Technical Project Manager
Apply for the
Software Engineering/Development: Clinical Outcome Technical Project Manager
role at
Canfield Scientific .
Job Description 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.
Responsibilities
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
Core Requirements
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
Desired
Knowledgeable of the software development life cycle
PMP Certification
Company Overview 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.
Salary Range $85,000 – $100,000 annually, dependent upon experience, education, and market conditions.
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Software Engineering/Development: Clinical Outcome Technical Project Manager
role at
Canfield Scientific .
Job Description 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.
Responsibilities
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
Core Requirements
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
Desired
Knowledgeable of the software development life cycle
PMP Certification
Company Overview 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.
Salary Range $85,000 – $100,000 annually, dependent upon experience, education, and market conditions.
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