Chiesi Farmaceutici S.p.A. is seeking a Clinical Operations professional based in Parma with hybrid/remote options. The role focuses on coordinating multiple clinical studies while ensuring quality, timelines, and...

Overview Are you looking for an impactful role within a growing business that helps advance science and improve human health? Would you enjoy the freedom of a field-based role where no two days are the same and you...

Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and...

Nurse for Home Visits for clinical trial patients Location: Padua Area Weekly working hours: around 1-3h per week Visits: weekly or every two weeks Contract duration: one year IQVIA is hiring an experienced Clinical...

Clinical Research Coordinator in Milano Working Hours 20 hours per week Start Date Immediately Duration Approximately 6 months IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a...

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Clinical Site Payment Associate Manager based in Italy. As a Clinical Site Payment...

Postdoctoral Position in Clinical Neurogenomics Italy Commitment & contract: collaboration contract, 12 months Location: Aosta (Italy) Step into a world of endless possibilities, together let’s leave something for the...

Are you being referred to one of our roles by a connection in Alira Health? If so, please apply using the referral link emailed to you. Join our global team dedicated to innovation and initiative, where physical walls...

Postdoctoral Position in Clinical Neurogenomics Italy Commitment & contract: collaboration contract, 12 months Location: Aosta (Italy) Step into a world of endless possibilities, together let’s leave something for the...

ESSENTIAL DUTIES AND RESPONSIBILITIES: Support CSTs in the setup, maintenance, and ongoing inspection readiness of the eTMF throughout the clinical study lifecycle. Collaborate with CROs and vendors to establish and...