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 across the group are united by a
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
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
Job Overview: The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Sr CRA
Job ID 514540 Posted since 17-Jul-2026 Organization Siemens Healthineers Field of work Sales Company Siemens Healthcare S.r.l. Experience level Mid-level Professional Job type Full-time Work mode Hybrid (Remote/Office) Employment type Permanent Location(s) Milan - Milano -
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
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
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
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
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,
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
ADECCO ITALIA SPA Ricerca per importante azienda cliente del settore farmaceuticoSTUDY COORDINATOR Attivita principali Supporto al team sperimentale nella fase di screening dei candidati allo studio; Supporto al team sperimentale nella fase di arruolamento dei soggetti in
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:
Global R&D QA, Senior Validation, Digital & Data Integrity Specialist Date: 22 Jul 2026 Department: Global R&D Quality Assurance Business Area: Quality Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT About us Chiesi is an
Specialty Care Coordinator - Wellness Village Part Time #26-316 Philadelphia, Pennsylvania, United States Locations(s) 7979 State Road, Philadelphia , Pennsylvania 19136 , United States Compensation $20.73 Job Description We need hope-bringers and changemakers - because the work
Job Purpose The Clinical Trial Liaison Manager (CTLM) is responsible for site performance, trial delivery and Sponsor oversight across assigned countries. The CTLM ensures timely, high‑quality clinical trial execution, with a strong focus on patient recruitment, protocol adherence,