Clinical Trial Site Start-Up Expert

Fortrea is seeking a Site Start-Up Specialist to coordinate site start-up activities, manage essential documents, and ensure timely regulatory submissions. You will interact with sites, sponsors, and authorities to maintain compliant, audit-ready records.The role requires 2+ years in clinical research or start-up processes, strong ICH/GCP knowledge, and...

CTI Clinical Trial and Consulting Services in Milano, Italy, seeks a Regulatory Affairs Administrator to manage country-level submissions for Clinical Trials and RWE, coordinating with Ethics Committees and Competent Authorities.The role requires 1-2 years in Clinical Research with regulatory exposure and fluency in Italian and English. You will collaborate...

CTI Clinical Trial and Consulting Services in Milano, Italy, seeks a Regulatory Affairs Administrator to manage country-level submissions for Clinical Trials and RWE, coordinating with Ethics Committees and Competent Authorities.The role requires 1-2 years in Clinical Research with regulatory exposure and fluency in Italian and English. xysqume Per essere...

Job SummaryOur clinical activities are growing rapidly, and we are currently seeking a full-time Clinical Trial Site Relationship Coordinator to join our vibrant Clinical Operations team in Italy, Milan. This is a fantastic opportunity to work on pre-award and post-award study feasibilities, build and maintain strategic relationships with our network of...

Please submit your application in English What You'll Do:Informs the RASSU department about any change of Drug Law/guidelines and updated requirements for submission on the country levelReview/prepare local submission documents and performs submissions (Initial submissions, Substantial Amendments and Notifications etc.) to Ethics Committees (Central and...

Chiesi in Nerviano (Milan) is seeking an experienced Secondary packaging Production Supervisor for a greenfield biologics project.Scopra se questa opportunità è adatta a lei leggendo tutte le informazioni riportate di seguito.You will oversee daily packaging operations and contribute to design, start-up, and validation activities to ensure GMP compliance...

Fortrea seeks a Site Start-Up Specialist to coordinate start-up activities, manage essential documents, and ensure timely regulatory submissions. You will join the FSPx team and work with a renowned sponsor to advance development of innovative therapies.In this role you will ensure audit-ready documentation, collaborate with cross-functional teams, and...

Chiesi Farmaceutici S.p.A.Sia tra i primi a candidarsi: legga la panoramica completa del ruolo qui sotto, quindi invii la sua candidatura per essere preso/a in considerazione.in Milan is seeking an experienced Sterile Production Supervisor to join a greenfield biologics operation.You will oversee aseptic processing, participate in design, start-up, and...

Senior Global Project Manager ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and...