Associate Manager, Clinical Trials Regulatory Management

Associate Manager, Clinical Trials Regulatory Management (m/w/d) Home based, EMEA Lisboa Associate Manager, Clinical Trials Regulatory Management (m/w/d)Home based, EMEALisboa Lisbon, Lisbon, Portugal Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects....

Regulatory Manager, Clinical Trials Regulatory ManagementHome based, EMEA Lisboa Regulatory Manager, Clinical Trials Regulatory ManagementHome based, EMEALisboa Lisbon, Lisbon, Portugal Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programs...

Overview:TFS HealthScience is excited to be expanding our SRS team and we are looking for an experienced, highly motivated CLINICAL TRIAL ASSOCIATE who shares our vision of providing clinical research excellence. Our SRS team is a highly experienced international group of professionals led by an industry expert.We are a leading global mid-size Contract...

Overview:TFS HealthScience is excited to be expanding our SRS team and we are looking for an experienced, highly motivated Clinical Trial Associate (CTA) who shares our vision of providing clinical research excellence. Our SRS team is a highly experienced international group of professionals led by an industry expert.We are a leading global mid-size Contract...

Clinical Trial Administrator, Single Sponsor dedicated Job Overview: CTA performs daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. By assisting in the coordination and administration of the study activities from the start up...

Senior Global Clinical Trial Assistant- Portugal Lisboa Senior Global Clinical Trial Assistant- PortugalLisboa Lisboa, Lisboa, Portugal col-wideJob Description:Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential...

Senior Global Clinical Trial Assistant- Portugal LisboaSenior Global Clinical Trial Assistant- PortugalLisboaLisboa, Lisboa, Portugalcol-wideJob Description:Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential...

Senior Global Clinical Trial Assistant- Portugal Lisboa Senior Global Clinical Trial Assistant- PortugalLisboaLisboa, Lisboa, Portugal col-wideJob Description:Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential...

col-wideJob Description:Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining...

Senior Global Clinical Trial Assistant- Portugal page is loaded Senior Global Clinical Trial Assistant- Portugal Apply locations Lisbon, Portugal time type Full time posted on Posted 2 Days Ago job requisition id R Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a...

Job Description:Transmission of practical skills and knowledge through on-the-job training in Clinical Trial Operations and Regulatory Support, such as:Prepare clinical trials' initial submissions, substantial amendments and notifications to the National Health Authority and Independent Ethics Committee.Support the negotiation of Clinical Trial Research...

Join us in our exciting journeyIQVIA is expanding in EMEA We currently have a Regional CPM to work sponsor-dedicated to one of our pharmaceutical clientsThe Clinical Trial Manager (CTM) is accountable for the operational and scientific oversight, the set-up, execution and delivery of their assigned clinical trials at the regional/local level. CTMs contribute...

Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.Essential Functions• Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and...

Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.Essential Functions• Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and...

Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.Essential Functions• Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and...

As a Clinical Trial Manager sponsor dedicated you will be primarily accountable for the end to end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations, sponsor's policies and procedures, quality standards and adverse event reporting requirements internally and externally.For certain...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas.With over 19,000 staff...

Are you an experienced Clinical Research Associate (CRA) looking for a new opportunity? Are you looking to advance your career in a dynamic and supportive environment? We have an exciting opportunity for you to join our team, based in either Lisbon or Porto Join our team as a Clinical Research Associate and contribute to the development of life-changing...

Junior Clinical Trial Administrator - FSP Team - Lisbon (Hybrid Position) page is loaded Junior Clinical Trial Administrator - FSP Team - Lisbon (Hybrid Position) Apply locations Lisbon Portugal time type Full time posted on Posted 6 Days Ago job requisition id As a leading global contract research organization (CRO) with a passion for scientific rigor and...