Software Engineering/Development: Clinical Outcome Technical Project Manager

Canfield Scientific; Bielefeld; Vor Ort; EUR 71.000 - 85.000; Vollzeit

Zusammenfassung

A leading medical technology firm in Bielefeld seeks a Clinical Outcome Technical Project Manager to oversee the design and deployment of eCOA systems across global clinical trials. The candidate must have a Bachelor’s degree, at least 3 years of relevant experience, and strong knowledge of clinical outcome assessments. Responsibilities include managing projects, collaborating with clinical operations, and developing project documentation. Comprehensive benefits and competitive salary offered.

Leistungen

Paid days off

Medical, dental, and vision insurance

Discretionary bonus

401(k) plan with employer match

Qualifikationen

• At least 3 years related experience in system development.
• Familiarity with regulatory requirements for clinical trials.
• Strong written and verbal communication skills required.

Aufgaben

• Manage design and deployment of eCOA and PRO systems.
• Collaborate with clinical operations and regulatory affairs.
• Develop mockups and interface with development teams.
• Document project status and metrics for stakeholders.
• Support postmortem reviews and improvement initiatives.

Kenntnisse

Strong knowledge of clinical outcome assessments (COAs)

eCOA platforms

Digital health technologies

Communication skills

Proficient in Microsoft operating systems

Knowledgeable of the software development life cycle

Ausbildung

Bachelor’s degree or equivalent

PMP Certification

Jobbeschreibung

Software Engineering/Development: Clinical Outcome Technical Project Manager

The ideal candidate for ourClinical Outcome Technology Project Manager position has great communication skills, is self-motivated and passionate about their work, has a strong desire to grow professionally, possesses an eagerness to be part of a dynamic group of focused and creative individuals and has 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 ideal candidate has deep expertise in clinical research operations, regulatory frameworks, and digital health technologies used in drug and device development.

Job Description:

• 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
• Responsible for developing mockups, writing software requirements, and interfacing directly with development teams
• Communicate status, issues, barriers, metrics, reports, and any other required/requested information to stakeholders as appropriate 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 systemsStrong 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 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 $85,000 - $100,000 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.

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