Project Manager (Medical Devices)
Pubblicato il 28-10-2026 - ClinOpsHub in Brindisi
Location : Mesagne (BR), Italy
Working hours: Full-time
Contract : Employment contract under the Italian CCNL Commercio (starting from €24,000 gross annual salary).
The contract type will be defined based on the selected candidate's experience.
ClinOpsHub S.r.l., founded in **** by Stefano Lagravinese, is a Contract Research Organization (CRO) self-certified with AIFA since ****.
We are a key player in the clinical research sector, providing services to pharmaceutical companies, clinical sites, laboratories, and other CROs, with a strong focus on quality, innovation, and professional growth.
Role & Objectives
The selected candidate will be responsible for planning, coordinating, and overseeing clinical research projects on medical devices, ensuring compliance with timelines, budget, and applicable regulatory requirements.
The primary objective of this role is to ensure effective project execution, mitigate operational risks, and maintain high-quality standards in the management of clinical studies involving medical devices.
Previous experience in the creation and management of eCRFs is required.
Key Responsibilities
Overall management of clinical projects on medical devices and projects handled by the Clinical Operations Department
Coordination of project team operational activities
Primary point of contact for Sponsors and project stakeholders
Monitoring of timelines, project budget oversight, and cost control
Identification and management of project risks
Support in study start-up activities
Coordination of communication across functions and involved resources
Preparation and facilitation of internal and external project meetings
Support in deviation and CAPA management
Periodic reporting on project progress
Requirements
Degree in a scientific field (e.g., Biotechnology, Pharmacy, Chemistry and Pharmaceutical Technology, Biomedical Engineering, or related)
At least 1 year of experience in clinical trial management
Proven experience in medical device projects
Knowledge of Good Clinical Practice (GCP)
Understanding of clinical trial management processes
Experience in project budget and timeline management
Familiarity with project risk management
Excellent command of English
What we offer
Continuous training and mentoring by senior professionals
Career growth opportunities in a young and dynamic environment
Possibility of hybrid working arrangements
Company benefits (welfare, meal vouchers, team building activities)
This job posting is open to candidates of all genders, ages, and nationalities (Italian Legislative Decree ******** and Directive *******/EC).
ClinOpsHub actively promotes diversity: equal qualifications considered, priority may be given to candidates from underrepresented groups within the team.
Privacy
Personal data will be processed in accordance with Regulation (EU) ******** (GDPR) and applicable data protection laws.
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