Clinical Research GBP Full Time jobs in Italy
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One thing we all have in common is the drive to produce great results for our clients and to advance treatment options available to patients worldw...
Your time here At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA’s are accountable for using...
The Site Activation Partner (SAP) is responsible for supporting operational activities related to site evaluation, activation, initiation, monitori...
The Clinical Contract Analyst serves as a legal liaison to process clinical contract requests such as but not limited to, Non-Disclosure Agreements...
Key Responsibilities: * Participates in site feasibility and/or pre-trial site assessment visits, providing recommendation from local area about site
Here at DOCS Global, we've entered into a partnership to supply an additional full-time, permanent home-based Independent CRAs to be aligned with a to
NONSTOP PARMA È ALLA RICERCA DI UN CLINICAL TRIAL MANAGER PER UNA DELLE AZIENDE LIFESCIENCE CON PIU' FORTE CRESCITA A FIRENZE.
At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission
UBC are looking for a SCRA who has experience of study start-up and is familiar with working in Italy. You may be working on late phase s
Clinical Project Manager/Local Study Manager positions available. Can you demonstrate proven track-record in: * Setting up and conducting national c
Director/Senior Director, Operational Strategy & Planning - Oncology The Director/Senior Director level of Operational Strategy& Planning (OS&P) i
Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, t
Are you an expert in Internal Medicine, Pulmonology or Rare Disease? Do you have an interest in the drug development process of novel therapeutics ...
Do you want to drive the development and commercialization of medicines that will provide treatment to patients with little or no alternate options...
As a member of the Study Start Up Team, you will play an integral role in making sure that physicians at our research sites are prepared to start the
I'm looking to speak with medical oncologists who are keen to join the pharmaceutical industry and support with oncology clinical trials!
Regulatory Start Up Specialist - CRO
Description: CROMSOURCE has a rare opportunity to join its team in Italy as a Clinical Project Manager for an internal position. The PM may act as
Quintiles and IMS Health have come together to become IQVIA, The Human Data Science Company™ Inspired by the industry we help, IQVIA commits to
This service provides global coordination for the execution for unblinded drug management, including the general facilitation of the Independent Dr...