Clinical Research Associate | Regulatory

As a Clinical Research Associate you will be expected to actively participate in and manage the recruitment of potential investigators and perform CA and EC submissions.You will be responsible for monitoring of clinical sites, maintenance of study files, conduct of pre-study, initiation visits, regular visits and close out visits and liaison with vendors and...

Meditrial is a full-service digital research organization with a foundation in clinical trial research, education, regulatory and market access. Meditrial has been leading the medical tech industry by delivering unparalleled outcomes for innovators. Our successful track record supporting medical device and biotechnology companies in all phases of clinical...

A leading global provider of clinical research services is seeking an Experienced Clinical Research Associate to monitor and manage clinical study sites based in Italy.The ideal candidate will have a Bachelor's degree and a Master's degree in a scientific field or health care, along with CRA certification.The role involves ensuring regulatory compliance,...

Una importante CRO in provincia di Milano ricerca un Clinical Research Associate (CRA) per un inserimento diretto a tempo indeterminato.Offriamo una retribuzione competitiva tra ****** e ****** euro, con opportunità di crescita professionale in un ambiente di medie dimensioni.Richiediamo laurea in discipline sanitarie, esperienza nel ruolo, e ottima...

Clinical Research Coordinator to support clinical research projects, ensuring regulatory compliance and managing research data.

Clinical Trial Manager – Italy | Advanced Clinical (FSP Model) Oncology focusedAdvanced Clinical is seeking an experienced Clinical Trial Manager to join our UK-based Functional Service Provider (FSP) team.This role will support global clinical studies and requires strong operational, vendor management, and monitoring oversight...

The Senior Clinical Research Associate (Senior CRA) is responsible for scheduling and conducting on-site and remote monitoring visits in compliance with applicable regulatory standards (MDR, ISO 14155, ICH/GCP guidelines, Teleflex procedures and IRB/EC policies and procedures). The Senior CRA conducts monitoring visits as identified by the monitoring plan,...

A global clinical research provider is seeking a Site Manager to oversee monitoring activities in clinical trials.Responsibilities include conducting site visits, ensuring regulatory compliance, and collaborating with study sites.The ideal candidate will have a Bachelor's and Master's degree in relevant fields, CRA certification, and experience in the pharma...

A global leader in applied safety science is seeking a UL GMA Knowledge Associate in Italy.The role involves completing comprehensive research reports, providing regulatory updates, and supporting business development by interpreting requirements and identifying new opportunities.Candidates should have at least two years of relevant experience and a high...

Clinical Research Coordinator II The Research Assistant supports the Department of Orthopaedic Surgery in the design, implementation, and administration of clinical research projects.This position works collaboratively with Principal Investigators (PIs), biostatisticians, residents, medical students, and other research staff to ensure regulatory compliance,...