offre-emploi

    Tous les emplois Clinical Trial Manager - ..


Quoi :    Où   :

298 offres d'emploi Clinical Trial Manager -


Clinical Trial Assistant

Lieu : Leuven Flanders
Société : Terumo

Job Responsibilities As a Clinical Trial Assistant,..you will be an essential part of our dynamic European Medical and Clinical Division at the EMEA HQ...

Postuler | Plus d'offres Clinical Trial Assistant
Plus d'offres - Leuven


Clinical Trial Assistant

Lieu : Leuven Flanders
Société : Terumo

focusing on the essential documents as per ISO14155 and Good Clinical Practice (GCP) guidelines...Join our team as a Clinical Trial Assistant and play a pivotal role in advancing medical research...

Postuler | Plus d'offres Clinical Trial Assistant
Plus d'offres - Leuven


Clinical Trial Assistant

Lieu : Leuven Flanders
Société : Terumo

Join our team as a Clinical Trial Assistant and play a pivotal role in advancing medical research...Sponsor Support: Play a pivotal role in setting up the Trial Master File (TMF)/electronic TMF for the Sponsor,..

Postuler | Plus d'offres Clinical Trial Assistant
Plus d'offres - Leuven


Clinical Trial Assistant

Lieu : Leuven Flanders
Société : Terumo

Ability to work with electronic Trial Master Files (eTMF),..you will be an essential part of our dynamic European Medical and Clinical Division at the EMEA HQ...

Postuler | Plus d'offres Clinical Trial Assistant
Plus d'offres - Leuven


Clinical Trial Assistant

Lieu : Leuven Flanders
Société : Terumo

..Reporting to the Clinical Operations Manager,..you will be an essential part of our dynamic European Medical and Clinical Division at the EMEA HQ...

Postuler | Plus d'offres Clinical Trial Assistant
Plus d'offres - Leuven


Clinical Trial Assistant

Lieu : Leuven Flanders
Société : Terumo

Reporting to the Clinical Operations Manager,..you'll be at the forefront of clinical research excellence,..

Postuler | Plus d'offres Clinical Trial Assistant
Plus d'offres - Leuven


Project Manager - FSP - Clinical Sample Manager

Lieu :
Société : Thermo Fisher Scientific

as well as PPD colleagues to deliver innovative clinical support.Discover Impactful Work:..Accountable for the development of realistic detailed study startup and monitoring plans as well as study deliveryAccountable for conducting country level feasibility in collaboration with Glo..

Postuler


Project Manager - FSP - Clinical Sample Manager

Lieu :
Société : Thermo Fisher Scientific

Study Managers may also input to and support compilation of sections to Clinical Study Reports.Will provide leadership to the teams in the setting of realistic recruitment targets and delivery milestones as the single point of accountability for detailed study start-up and mo..

Postuler


Project Manager - FSP - Clinical Sample Manager

Lieu :
Société : Thermo Fisher Scientific

as well as PPD colleagues to deliver innovative clinical support.Discover Impactful Work:..and assessing site activation plansLeads study risk planning process in context of site and subjectCoordinate study/protocol training & investigator meetingsDevelops and provides key inputs to..

Postuler


Project Manager - FSP - Clinical Sample Manager

Lieu :
Société : Thermo Fisher Scientific

etc.)Keys to Success:Education:MS/PhD – minimum of 3 years of proven experienceBS/Nurse – minimum of 5 years of proven experienceExtensive global clinical trial/study management experienceWorking knowledge of Good Clinical Practices,..

Postuler


Clinical Data Manager

Lieu : Bruxelles Brussels
Société : EORTC

with the close coaching of a Clinical Data Expert:Clinical trial protocolDevelopment of the Data Management sections of the clinical trial protocolAssisting in the final review of the clinical trial protocol for consistency and operational f..

Postuler | Plus d'offres Clinical Data Manager
Plus d'offres - Bruxelles


Clinical Data Manager

Lieu : Bruxelles Brussels
Société : EORTC

data cleaning and data reporting activitiesApplication of QC to each stage in the data handling to ensure the data are reliable and processed in compliance with ICH-GCP requirements.Communication with the participating investigators to resolve queries and collect missing dataPerforming the..

Postuler | Plus d'offres Clinical Data Manager
Plus d'offres - Bruxelles


Clinical Data Manager

Lieu : Bruxelles Brussels
Société : EORTC

data cleaning and data reporting activitiesApplication of QC to each stage in the data handling to ensure the data are reliable and processed in compliance with ICH-GCP requirements.Communication with the participating investigators to resolve queries and collect missing dataPerforming the..

Postuler | Plus d'offres Clinical Data Manager
Plus d'offres - Bruxelles


Clinical Project Manager

Lieu : Zaventem Flanders
Société : IQVIA

Partners with the Clinical Trial Assistant (CTA)/Investigator Document Assistant (IDA),..if delegated by FM.Ensure accurate finance reporting and trial delivered within budgetKeeps the trial in compliance with local regulatory requirements by organizing and ensu..

Postuler | Plus d'offres Clinical Project Manager
Plus d'offres - Zaventem


Clinical Data Manager

Lieu : Bruxelles Brussels
Société : EORTC

with the close coaching of a Clinical Data Expert:Clinical trial protocolDevelopment of the Data Management sections of the clinical trial protocolAssisting in the final review of the clinical trial protocol for consistency and operational f..

Postuler | Plus d'offres Clinical Data Manager
Plus d'offres - Bruxelles


Clinical Data Manager

Lieu : Bruxelles Brussels
Société : EORTC

review and validation of the clinical data promptly;..The Clinical Data Manager reports on study activities and status to the study team.The Clinical Data Manager is responsible for all the steps required for the setup of the Data Management tools of a
Postuler | Plus d'offres Clinical Data Manager
Plus d'offres - Bruxelles


Clinical Data Manager

Lieu : Bruxelles Brussels
Société : EORTC

The Clinical Data Manager will carry out the following tasks,..Share onThe Clinical Data Manager works under the hierarchical supervision of the Clinical Data Expert...

Postuler | Plus d'offres Clinical Data Manager
Plus d'offres - Bruxelles


Clinical Data Manager

Lieu : Bruxelles Brussels
Société : EORTC

The Clinical Data Manager reports on study activities and status to the study team.The Clinical Data Manager is responsible for all the steps required for the setup of the Data Management tools of a clinical trial and for the collection,..

Postuler | Plus d'offres Clinical Data Manager
Plus d'offres - Bruxelles


Clinical Data Manager

Lieu : Bruxelles Brussels
Société : EORTC

The Clinical Data Manager will carry out the following tasks,..review and validation of the clinical data promptly;..

Postuler | Plus d'offres Clinical Data Manager
Plus d'offres - Bruxelles


Clinical Data Manager

Lieu : Bruxelles Brussels
Société : EORTC

The Clinical Data Manager reports on study activities and status to the study team.The Clinical Data Manager is responsible for all the steps required for the setup of the Data Management tools of a clinical trial and for the collection,..

Postuler | Plus d'offres Clinical Data Manager
Plus d'offres - Bruxelles


Clinical Supply Chain Manager

Lieu : Rixensart Wallonia
Société : 1054 GlaxoSmithKline Services Unlimited

ICH and GCPs.Experience working with senior leadership including but not limited to Clinical Operations,..and CMC leadership.Project management experiencePreferred Qualifications:Understanding of the drug development process and experience with clinical supplies manufacturing..

Postuler | Plus d'offres Clinical Supply Chain Manager
Plus d'offres - Rixensart


Clinical Supply Chain Manager

Lieu : Rixensart Wallonia
Société : 1054 GlaxoSmithKline Services Unlimited

ICH and GCPs.Experience working with senior leadership including but not limited to Clinical Operations,..and procedures5+ years of experience working in pharmaceuticals.Experience in the management of clinical trial supplies including,..

Postuler | Plus d'offres Clinical Supply Chain Manager
Plus d'offres - Rixensart


Clinical Supply Chain Manager

Lieu : Rixensart Wallonia
Société : 1054 GlaxoSmithKline Services Unlimited

and CMC leadership.Project management experiencePreferred Qualifications:Understanding of the drug development process and experience with clinical supplies manufacturing and packagingAbility to maintain accurate records and files in accordance with cGMPs and SOPs.Ability to indepen..

Postuler | Plus d'offres Clinical Supply Chain Manager
Plus d'offres - Rixensart


Clinical Supply Chain Manager

Lieu : Rixensart Wallonia
Société : 1054 GlaxoSmithKline Services Unlimited

and supply planning of clinical trials.Experience working with global regulatory requirements,..This role supports Phase I through IV GSK sponsored clinical studies as well as investigator sponsored trials and compassionate use programs.Leads the cross-functiona..

Postuler | Plus d'offres Clinical Supply Chain Manager
Plus d'offres - Rixensart


Clinical Supply Chain Manager

Lieu : Rixensart Wallonia
Société : 1054 GlaxoSmithKline Services Unlimited

assumptions and constraints of the clinical supply chain and ensures supply options and risks are explored and agreedInfluences team decisions to maximize the use of resources/materials,..

Postuler | Plus d'offres Clinical Supply Chain Manager
Plus d'offres - Rixensart





















<< Précédents || Suivants >>




Recherche d'emploi par pays © 2025 Offres d'emploi fournis par offre-emploi ==>