study start up unit

Please submit your application in English WhatYou'llDo: Support of Regulatory Affairs Study Start-Up (RASSU) department: Informs the RASSU department about any change of Drug Law/guidelines and updated requirements for submission on the country level Review/prepare local submission documents and performs submissions (Initial submissions, Substantial...

Study Start Up Associate IIICON 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 suppliers.As...

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...

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. As a Study Start Up Associate II at ICON, you will lead the initiation of clinical trials,...

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. xbvzest Per essere...

Please submit your application in English WhatYou'llDo: Support of Regulatory Affairs Study Start-Up (RASSU) department: Informs the RASSU department about any change of Drug Law/guidelines and updated requirements for submission on the country level Review/prepare local submission documents and performs submissions (Initial submissions, Substantial...

Please submit your application in English Si candidi (facendo clic sul pulsante apposito) dopo aver controllato tutte le informazioni di lavoro riportate di seguito.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...

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 level Review/prepare local submission documents and performs submissions (Initial submissions, Substantial Amendments and Notifications etc.) to Ethics Committees (Central and...

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.Scopra esattamente quali competenze, esperienze e qualifiche sono necessarie per avere successo in...

Please submit your application in English What You'll Do: Support of Regulatory Affairs Study Start-Up (RASSU) department: Informs the RASSU department about any change of Drug Law/guidelines and updated requirements for submission on the country level Review/prepare local submission documents and performs submissions (Initial submissions, Substantial...

Study Start Up Associate IIICON 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...

Please submit your application in English Si candidi (facendo clic sul pulsante apposito) dopo aver controllato tutte le informazioni di lavoro riportate di seguito.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...

** Please submit your application in English **   What You'll Do: Support of Regulatory Affairs Study Start-Up (RASSU) department: Informs the RASSU department about any change of Drug Law/guidelines and updated requirements for submission on the country level Review/prepare local submission documents and performs submissions (Initial submissions,...

Study Start Up Associate IIICON 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 suppliers.As...

Ergomed Group in Italy is seeking a Senior Specialist in Study Start Up & Regulatory Affairs to lead and coordinate activities for site initiation readiness.Se le sue competenze, la sua esperienza e le sue qualifiche corrispondono a quelle descritte in questa panoramica, non ritardi l'invio della sua candidatura.You will ensure regulatory compliance and act...

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. As a Study Start Up Associate II at ICON, you will lead the initiation of clinical trials,...

Ergomed Group in Italy is seeking a Senior Specialist in Study Start Up & Regulatory Affairs to lead and coordinate activities for site initiation readiness.Se le sue competenze, la sua esperienza e le sue qualifiche corrispondono a quelle descritte in questa panoramica, non ritardi l'invio della sua candidatura.You will ensure regulatory compliance and act...

Ergomed seeks a Senior Specialist, Study Start Up and Regulatory Affairs to lead and coordinate activities to achieve site initiation readiness.Non si lasci sfuggire questa opportunità: si candidi rapidamente se la sua esperienza e le sue competenze corrispondono a quanto descritto di seguito.You will provide regulatory expertise, ensure compliance, and act...

CTI is seeking a Regulatory Affairs Start-Up professional in Milan to support the RASSU department with submissions, country-specific requirements, and document preparation. You will liaise with Ethics Committees, Competent Authorities, and the CTI Legal team to ensure timely, compliant submissions across country sites. Strong Italian and English, plus...

Ergomed Group in Italy seeks a Senior Specialist, Study Start Up and Regulatory Affairs to lead activities ensuring site initiation readiness across studies.Il suo CV è pronto? Se sì, e se è convinto/a che questo sia il ruolo giusto per lei, si candidi il prima possibile.You will provide subject matter expertise, manage regulatory submissions, and liaise...