Global Regulatory Submissions Specialist

Overview Within the Global Regulatory Affairs Operations department, whose mission is to provide timely and high-quality regulatory submission-ready packages to facilitate faster time to market, while driving business solutions that support the company's cross-functional processes and advancing company's digital capabilities, the resource, reporting...

Overview Within the Global Regulatory Affairs Operations department, whose mission is to provide timely and high-quality regulatory submission-ready packages to facilitate faster time to market, while driving business solutions that support the company’s cross-functional processes and advancing company’s digital capabilities, the resource, reporting to...

European Union North America Middle East (GCC/MENA) Africa Asia-Pacific (APAC) China (NMPA) JSB Solutions – azienda leader nei servizi life sciences con focus su consulenza, gestione studi clinici e sviluppo software – ricerca per il potenziamento del proprio organico un Global Regulatory Affairs Senior Specialist (JSB.SRF.26.023) da...

JSB Solutions cerca una figura Senior Specialist Global Regulatory Affairs per potenziare la divisione Regulatory Affairs. Il ruolo richiede autonomia, gestione di progetti regolatori complessi e coordinamento con stakeholder internazionali. Si lavorerà su strategie regolatorie UE ed extra-UE, con possibilità di trasferte nazionali. Si richiede almeno 6...

Drive the regulatory strategy, planning and execution across key regions for the assigned development pipeline projects (from early preclinical phases)Collaborate with cross-functional teams to ensure timely submissions, approvals, and compliance with global regulatory requirements, supporting the successful development and registration of innovative...

Hire Feed is hiring a Biostatistician to work remotely on a full-time basis, analyzing clinical trial data and designing statistical methodologies for regulatory submissions. The role requires SAS/R/Python proficiency, experience with clinical trials and FDA/EMA guidelines, and the ability to communicate complex results to non-statistical stakeholders. This...

OverviewQuality Assurance Regulatory Affairs (QARA) Specialist – Dedalus. Remote in Italy. Part of the Global Quality and Assurance Team to drive quality and regulatory excellence in healthcare technology.What you’ll achieveAs a QARA Specialist you will ensure compliance with Quality and Regulatory standards across the company, contributing to better...

Select how often (in days) to receive an alert:Alfasigma is a privately held global healthcare company founded over 75 years ago in Italy, where it remains headquartered today in Bologna and Milan. The Group operates in over 100 markets spanning Europe, North and South America, Asia, and Africa.Over three years ago, we embarked on a transformative journey to...

IQVIA is seeking a Global Site Activation Manager for a homebased position. You will lead strategic, operational, and financial delivery of site activation across studies and regions to accelerate patient enrollment.You will oversee site identification, ethics/regulatory submissions, and contracting, ensuring alignment with sponsor and IQVIA requirements,...