Project Manager (Medical Devices)

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7c6bvj

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 2014 by Stefano Lagravinese, is a Contract Research Organization (CRO) self-certified with AIFA since 2019.

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 198/2006 and Directive 2000/78/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) 2016/679 (GDPR) and applicable data protection laws.

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Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7c6bvj