When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
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
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Clinical Trial Coordinator – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Clinical Trial Coordinator – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750
With its beginnings in a family run pharmacy in Correggio, Italy in the 1920s, Recordati is now a global pharmaceutical company, listed on the Italian stock exchange, with over 4,500 employees and turnover of over Euro
A global pharmaceutical company in Turbigo is seeking a TMF Specialist to manage clinical documentation processes. The successful candidate will oversee the Trial Master File, ensure regulatory compliance, oversee CRO activities, and improve documentation strategies. Candidates should
Descrizione dellazienda About AbbVie La missione di AbbVie Italia è scoprire e offrire soluzioni e terapie innovative che rispondano alle principali sfide di salute di oggi e di domani. Il nostro impegno è generare un impatto
A Proposito di TMF Group TMF Group è un provider di servizi amministrativi che aiuta i propri clienti ad investire ed operare in sicurezza in tutto il mondo. I nostri 11.000 esperti presenti in 87 nazioni con 125+
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
Job Summary The Clinical Study Manager (CSM) will be part of the Clinical Operations Department, which is responsible for planning, executing, managing and closing studies associated with the company clinical development plans. The CSM is a
Parexel is pleased to announce we are looking to hire several CRA II for the team in Italy. Candidates must have close to atleast 2 years independent monitoring experience in a similar setting. The role can
Experienced Clinical Research Associate, IQVIA Biotech - Home based, Italy 1 day ago Be among the first 25 applicants Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and
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
Discover the Role The primary responsibility of the Associate Accountant is to work with the Supervisor/Coordinator/Senior Accountant in meeting the accounting, tax and other reporting commitments of the relevant clients. She/he is responsible for individual goals
Overview We’re building the future of how the world communicates. Netcracker, part of NEC Corporation, combines deep telecom industry expertise with cutting-edge cloud-native and AI-powered innovations to enable communications service providers and enterprises to transform their
The Clinical Study Manager (CSM) will be part of the Clinical Operations Department, which is responsible for planning, executing, managing and closing studies associated with the company clinical development plans. The CSM is a proven leader
TMF Group is seeking interns for the Accounting & Tax department in Milano, Italy. As an intern, you will be involved in diverse projects related to accounting, tax, and reporting for well-known local and international companies. This
Experteer OverviewAs a Clinical Research Associate, you monitor and manage study sites to ensure protocol adherence, regulatory compliance, and timely data reporting. You will work with sites to optimize recruitment, train investigators, and maintain essential study
Experteer OverviewIn this CRA role, you will independently conduct site monitoring for clinical trials and provide guidance to the monitoring team to ensure compliance and quality. You will collaborate with cross-functional teams to address site questions,
Overview Join us in redefining what it means to work for a CRO. When you work at Rho, its more than just a job—you become part of the Rho Factor. Were a proud bunch of science