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Working at ClinOpsHub
Join our team
ClinOpsHub was registered in 2019 as a Contract Research Organization (CRO) on the Italian Competent Authority platform (Agenzia Italiana del Farmaco – AIFA), in compliance with the Italian Ministerial Decree of 15 November 2011.
Our team is dynamic, flexible, highly available, and always updated with the latest regulatory standards, providing responsive and efficient support tailored to project’s needs of the Client.
Open positions:
Responsible Person for Pharmacovigilance
We are looking for an experienced Responsible Person for Pharmacovigilance with a strong background in pharmacovigilance activities within clinical trials.
Training Project Coordinator (Internship)
We are looking for a candidate to join our Clinical Operations Department as an intern, with a strong interest in gaining hands-on experience in the operational and documentation-related management of clinical studies.
Training Project Coordinator (Internship)
We are looking for a candidate to join our Training Department as an intern, interested in gaining hands-on experience in the organization and management of training projects, scientific communication, and activities aimed at promoting our training offer.
Administrative Officer (Internship)
We are looking for a candidate to join our Administration Department as an intern, interested in gaining hands-on experience in the main administrative, accounting, and management activities within a corporate environment.
Junior Marketing Specialist – Internship
ClinOpsHub is looking for a junior resource as a Marketing Specialist to support activities related to corporate brands and training projects dedicated to the pharmaceutical and clinical research sector.
Junior IT Specialist - Intership
Project Manager (Medical Devices)
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.
Quality Assurance (with GCP qualification)
In view of the imminent increase in projects in the area of quality assurance for clinical trials, we plan to strengthen the Quality Assurance Department. We are therefore looking for a resource to support ClinOpsHub’s Quality Assurance Consultants in managing department projects, in accordance with company SOPs, guidelines, and national and international regulations. The selected resource will travel to customer sites and serve as a direct point of contact with them.
Course Assistant (“Missione CRA” Training Program)
To support the dissemination of our company’s mission, we are looking for a dynamic, motivated, and eager-to-learn individual to join our team for the entire duration of the “Missione CRA” training course, at the ClinOpsHub office located in Mesagne (BR).