Regulatory Submissions Coordinator

Job Summary: Our clinical operations activities are growing rapidly and we are currently seeking full-time, **Regulatory Submissions Technical Advisors** to join our Site Activation and Maintenance team, within Clinical Operations. This position plays a key role at Medpace, preparing and reviewing regulatory documents and providing strategic regulatory...

Company Description PSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. **Job Description**: Join our team of experts in regulatory...

IQVIA MedTech Clinical Solutions, specializes in clinical research for Medical Devices and In-Vitro Diagnostic (IVD) products. IQVIA MedTech’s focused expertise meets the growing needs of device Sponsors to justify product safety and effectiveness as well as reimbursement and adoption challenges due to increased scrutiny by regulators, end-users, and...

**Regulatory Affairs Specialist (maternity leave)** At AstraZeneca we believe in the potential of our people and you’ll develop beyond what you thought possible. We make the most of your skills and passion by actively supporting you to see what you can achieve no matter where you start with us. As **Regulatory Affairs Specialist (maternity leave)** in...

Manpower divisione Onsite ricerca per un’importante azienda operante nella produzione e confezionamento conto terzi di integratori alimentari, dispositivi medici, un/una: Regulatory Affair Coordinator - Medical Devices La risorsa si occuper di: Gestione dei processi regolatori per la registrazione di Integratori Alimentari (Direttiva 2002/46/EC,...

Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. At least 3 years' experience with submissions. Italian...

Manpower divisione Onsite ricerca per un’importante azienda operante nella produzione e confezionamento conto terzi di integratori alimentari, dispositivi medici, un/una: Regulatory Affair Coordinator - Medical Devices La risorsa si occuper di: Gestione dei processi regolatori per la registrazione di Integratori Alimentari (Direttiva 2002/46/EC,...

Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. At least 3 years' experience with submissions. Italian...

Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. At least 3 years' experience with submissions....

ABOUT THE ROLE: Relative to the Italian market, the AML and Compliance Coordinator contributes to the establishment of a corporate culture which respects the principles of compliance, the principles identified in Fides procedures and in the code of ethics drawn up by Crédit Agricole S.A. through specific training programs. Additionally, the Coordinator...

ABOUT THE ROLE: Relative to the Italian market, the AML and Compliance Coordinator contributes to the establishment of a corporate culture which respects the principles of compliance, the principles identified in Fides procedures and in the code of ethics drawn up by Crédit Agricole S.A. through specific training programs. Additionally, the Coordinator...

**Labcorp Drug Development** As a leading contract research organization (CRO), Labcorp Drug Development provides comprehensive drug development solutions for a range of industries. Our services cover the preclinical, clinical and post-market phases of drug development, the product life cycles for medical device and diagnostics and development services...

On behalf of our Client a global pharmaceutical company, IQVIA is looking for a **Statistical Programmer **who can join an exciting working environment in a dynamic atmosphere. **JOB DESCRIPTION**: - To develop SAS programs and statistical output for the management and reporting of clinical trial data managed by GCD. - To guarantee quality of statistical...

Invia un messaggio diretto all’autore dell’offerta di lavoro da BFF Banking Group BFF Bank è una realtà bancaria presente sul mercato da circa 40 anni, quotata in Borsa Italiana e in continua crescita ed espansione. È il più grande operatore di finanza specializzata in Italia, nonché leader in Europa nella gestione e nello smobilizzo pro soluto di...

**Primary contact and liaison with investigative sites during study maintenance and -when assigned-, site start-up activities, with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB submissions are made within the timelines agreed with project management and Start-up team.**: - ** Collect, track...

**Labcorp Drug Development** is looking to hire a **Clinical Trial Coordinator** in Italy. In this position, you will be fully dedicated to a **single sponsor** and you will have a **full-time** **and **permanent** **contract**. As a Labcorp Drug Development employee dedicated to an FSP project, you will bring your specialized discipline to a core team...

**Start Up - Specialist**: - ** Minimum 1 year of experience working as Start - Up Specialist.**: - ** Serve as local expert in project start-up activities for a particular country or region.**: - ** Act as a ‘knowledge resource’ to mentor and train new hires and less-experienced department colleagues.**: - ** Collect, track and perform a quality...

Job Description As a  Clinical Research Associate  at PSI Italy you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry. Hybrid working arrangement in Milan area or homebased in other regions of Italy Responsibilities: Conduct and report all...

Lead Statistical Programmer (Italia) page is loaded Lead Statistical Programmer (Italia) Apply locations Milan, Italy time type Full time posted on Posted 30+ Days Ago job requisition id R1377059 On behalf of our Client a global pharmaceutical company, IQVIA is looking for a Statistical Programmer who can join an exciting working environment in a...

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 sponsor requirements. Essential Functions Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with...