On behalf of our Client, Chiesi Farmaceutici, one of the top 50 pharmaceutical companies in the world with more than 80 years of experience in the pharmaceutical and biotechnology industry, IQVIA is looking for a Clinical Project
On behalf of our Client, Chiesi Farmaceutici, one of the top 50 pharmaceutical companies in the world with more than 80 years of experience in the pharmaceutical and biotechnology industry, IQVIA is looking for a Clinical Project
JOB DESCRIPTION: 1. Summary of Position The Territory Manager is responsible for driving sustainable growth in the advanced heart failure business by developing LVAD programs, expanding implanting centers, and optimizing patient identification and referral pathways across
Introduction to the Role: Are you ready to transform real-world data into evidence that changes clinical practice and access decisions? Does it motivate you to see how a well-designed evidence project can improve patients’ treatment journeys and inform
L’Istituto Clinico Scientifico Maugeri cerca un Clinical Data Manager/Study Coordinator per gestire i dati clinici di uno studio prospettico. Interverrai in collaborazione con i team di ricerca interdisciplinari, assicurando integrità e coerenza dei dati. Competenze in e-CRF e gestione
Clinical Data Manager/Study Coordinator-Progetto di ricerca La figura selezionata svolgerà i seguenti compiti: Raccolta, verifica, inserimento, aggiornamento e gestione dei dati clinici relativi al clinical trial prospettico in oggetto, in collaborazione con i team interfunzionali di ricerca partecipanti al progetto;
Job Description Summary The RN Clinical Coordinator oversees daily clinical operations within a hospital unit or department, ensuring high-quality patient care, efficient workflow, and effective communication among multidisciplinary teams. This role bridges clinical practice and administrative functions to enhance patient
IQVIA in Modena, Italy, is seeking a Data Operations Coordinator to provide foundational and intermediate data management expertise within the Clinical Data Management team. You will support the delivery of compliant data outputs meeting customer requirements. Responsibilities include data review, queries resolution, database
Research Nurse/Clinical Research Coordinator (Part-time, On-site, Independent Contractor) Novara Italy RapidTrials is hiring an experienced Clinical Research Coordinator (CRC) to support prescreening and recruitment activities for a Phase III MASH (Metabolic Dysfunction-Associated Steatohepatitis) clinical trial. This part‑time, freelance role is based
Direct message the job poster from Philogen S.p.A. Philogen S.p.A. is a biotechnology company whose mission is the development of biologic products for the imaging and therapy of life‑threatening diseases, with a strategic focus on cancer
Business Area: R&D, Pharmacovigilance & Regulatory Affairs About us Chiesi is an international research‑focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees
Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a singular purpose:
Experteer Overview As a CTLM, you act as Recordati’s sponsor representative at site level, driving trial delivery and strong PI/site partnerships. You will support site start-up, recruitment, and Sponsor oversight of CRO activities to ensure compliant,
On behalf of our Client, Chiesi Farmaceutici , one of the top 50 pharmaceutical companies in the world with more than 80 years of experience in the pharmaceutical and biotechnology industry, IQVIA is looking for a
ID: 2525 Date of Posting: Apr 27, 2026 Business Area: Research & Development Job Type: Direct Employee Territory: Full-Time or Part-Time: Full Time Seniority: Mid-senior With its beginnings in a family run pharmacy in Correggio, Italy
Job Overview Provide foundational and intermediate-level data management expertise to the Clinical Data Management (CDM) team. Support the delivery of high-quality, compliant, and efficient data management outputs that meet internal and external customer requirements. May also contribute to team leadership
Experteer Overview In this CRA role, you contribute to the development and oversight of drugs and medical devices by conducting site visits and ensuring compliance with protocols and regulations. You work within a team of therapeutic
Experteer Overview In this role you will contribute to the growth of our clinical monitoring activities in Italy as part of a collaborative team. You will conduct site visits, verify qualifications and resources, and ensure data quality and
Experteer Overview In this role you support Medpace’s clinical monitoring efforts across Italy, enabling high-quality, compliant trials. You will join a cross-functional team to conduct site visits, verify data and investigator qualifications, and ensure regulatory adherence. The position
Experteer Overview In this CRA role at Medpace you will support the integrity of clinical studies across pharmaceutical and medical device development. You’ll join a training-focused program (PACE) that accelerates your skills toward independent CRA responsibilities. You