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298 offres d'emploi Clinical Trial Manager -


Clinical Trial Assistant

Lieu : Leuven Flanders
Société : Terumo

Capacity to work effectively with project managers,..Quality Assurance: Review applicable clinical study plans and create or support the development of a Trial Master File plan for each clinical study...

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


Clinical Trial Assistant

Lieu : Leuven Flanders
Société : Terumo

Quality Assurance: Review applicable clinical study plans and create or support the development of a Trial Master File plan for each clinical study...

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


Clinical Trial Assistant

Lieu : Leuven Flanders
Société : Terumo

you'll be at the forefront of clinical research excellence,..Investigator Site File (ISF): Prepare the ISF during the activation phase of clinical studies,..

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


Clinical Trial Assistant

Lieu : Leuven Flanders
Société : Terumo

you'll have the opportunity to engage in meaningful conversations with the hiring manager and other enthusiastic Terumo associates...

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),..ensuring the success of clinical studies...Capacity to work effectively with project managers,..

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...Capacity to work effectively with project managers,..

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


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


Project Manager - FSP - Clinical Sample Manager

Lieu :
Société : Thermo Fisher Scientific

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 Global Clinical Trial Execution and CROs,..

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:..may be required to act as ‘lead’ study manager,..

Postuler


Project Manager - FSP - Clinical Sample Manager

Lieu :
Société : Thermo Fisher Scientific

and will coordinate activities of the other Study Managers assigned.A day in the Life:..digital and decentralized clinical trial services...

Postuler


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 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

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

if delegated by FM.Ensure accurate finance reporting and trial delivered within budgetKeeps the trial in compliance with local regulatory requirements by organizing and ensuring IEC/HA approvals in cooperation with the local Start Up team,..

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


Clinical Data Manager

Lieu : Bruxelles Brussels
Société : EORTC

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

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

..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

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

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

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 Supply Chain Manager

Lieu : Rixensart Wallonia
Société : 1054 GlaxoSmithKline Services Unlimited

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

This role supports Phase I through IV GSK sponsored clinical studies as well as investigator sponsored trials and compassionate use programs.Leads the cross-functional Clinical Supply Chain Network team and is accountable for the Clinical Supply Workstream as pa..

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


Clinical Supply Chain Manager

Lieu : Rixensart Wallonia
Société : 1054 GlaxoSmithKline Services Unlimited

The SCM is accountable for determining supply strategies that successfully deliver investigational medicines to patients while ensuring the supply chain delivers results that support GSK R&D registration & launch milestones.The SCM is responsible for influencing clinical plans relat..

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,..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 resourc..

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





















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