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Senior principal engineer, investigator and patient solutions

Anvers
TN Belgium
De 80 000 € à 100 000 € par an
Publiée le 24 mai
Description de l'offre

Job Title:

Senior Principal Engineer, Investigator and Patient Solutions, Beerse


Client:

Johnson and Johnson


Location:

Beerse, Belgium


Job Category:

Other


EU work permit required:

Yes


Job Reference:

75b0a2794a30


Job Views:

3


Posted:

22.05.2025


Expiry Date:

06.07.2025


Job Description:

Johnson & Johnson is committed to health and innovation, aiming to prevent, treat, and cure complex diseases, with smarter and less invasive treatments tailored to individual needs. Our expertise spans Innovative Medicine and MedTech, enabling us to develop healthcare solutions that make a profound impact on human health.

We are recruiting for a Senior Principal Engineer to provide strategic and operational leadership in patient and site-facing solutions related to resource, budget, and portfolio management. This role involves coordinating technical operations, managing stakeholder interfaces, ensuring regulatory compliance, and leading project and team management efforts. The position supports the growth of our Digital R&D capabilities and may include people management responsibilities, including hiring, performance management, and fostering an inclusive environment.

Responsibilities include:

* Leading high-impact technology projects to improve clinical trial processes and patient engagement.
* Managing a diverse team to ensure inspection-ready practices and stakeholder value.
* Identifying emerging technologies and opportunities for innovation.
* Maintaining customer satisfaction and regulatory compliance.
* Managing financial plans and resource allocation.
* Applying project management best practices.
* Developing technology roadmaps aligned with strategic goals.
* Representing the department during audits and inspections.
* Providing leadership in hiring, mentoring, and talent development.

Qualifications:

* Bachelor’s degree in Health, Science, IT, or related field.
* At least 8 years of relevant experience in clinical trial operations, preferably in pharma, medical devices, or CROs.
* Proficiency with IT systems supporting clinical development and reporting tools.
* Understanding of drug development processes and GCPs.
* Experience with learning management systems.
* Project management certification is preferred.
* Excellent communication, problem-solving, and global mindset.
* Ability to influence across a matrix organization.
* Willingness to travel approximately 10% domestically and internationally.
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