Project Manager (Medical Devices)

ClinOpsHub; Brindisi; In loco; EUR 22.000 - 26.000; Tempo pieno

Vantaggi offerti da questo lavoro

Hybrid work

Training & mentoring

Career growth

Welfare benefits

Descrizione del lavoro

ClinOpsHub S.r.l. is recruiting for a Clinical Operations role focused on managing clinical projects for medical devices. You will plan, coordinate, and oversee studies, ensuring compliance with timelines, budgets, and regulatory requirements.

The ideal candidate has at least 1 year of clinical trial management experience, with strong English language skills and a background in a scientific field. Hybrid working arrangements are offered.

Competenze

• GCP knowledge required.
• 1 year of experience in clinical trial management.
• Familiarity with medical device projects.
• Excellent command of English.

Mansioni

• Overall management of clinical projects on medical devices.
• Coordinate project team operational activities and timelines.
• Be the primary contact for Sponsors and stakeholders.
• Monitor budget and timelines, manage risks.

Conoscenze

GCP knowledge

Clinical trial management

Budget & timeline management

Risk management

English proficiency

Formazione

Degree in a scientific field (Biotechnology, Pharmacy, Chemistry & Pharmaceutical Technology, Biomedical Engineering, or related)

Descrizione del lavoro

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.