158 offres d'emploi Global Clinical Study Manager - |
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Lieu : Montpellier
Société : Excelya
- Oversee study monitoring activities and follow-up by controlling quality (frequency of monitoring visits,..as Global Study Manager,..
Postuler | Plus d'offres Global Clinical Study Manager
Plus d'offres - Montpellier |
Lieu : Paris
Société : Excelya
implements corrective actions in conjonction with Study Team / Project Team and escalate to the DM Program Lead when necessary...
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Lieu : Pusignan Auverge-Rhône-Alpes
Société : Stryker
consultants and vendors.You will track and report on the progress of assigned clinical trials including budget and timelines.You will collaborate and work with Clinical Trial Managers,..
Postuler | Plus d'offres Sr. Clinical Study Manager
Plus d'offres - Pusignan |
Lieu : Bordeaux Nouvelle-Aquitaine
Société : Intuitive Surgical
Manages ongoing study activities,..The purpose of this job function is to serve as a Clinical Project Manager (CPM) in the Clinical Affairs Department to support projects in Europe (EU)...
Postuler | Plus d'offres Clinical Study Manager
Plus d'offres - Bordeaux |
Lieu : Gif-sur-Yvette Île-de-France
Société : Danone
Short Intro and About the Job Le département Medical & Nutritional Science recrute un.e Clinical Study Manager (H/F) en CDI dans l'équipe Clinical Research & Health Data...
Postuler | Plus d'offres CDI - Clinical Study Manager (H/F)
Plus d'offres - Gif-sur-Yvette |
Lieu : France
Société : Excelya
ambitious health company on the path to becoming the clinical research leader in Europe thanks to our 800 Excelyates...
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Lieu :
Société : MicroVention
set enrollment targets and implement enrollment and mitigation plans.Work with legal team to facilitate preparation of clinical trial agreements,..
Postuler | Plus d'offres Clinical Research Manager, EMEA |
Lieu : Paris
Société : Meet
Ensure timely and accurate submission of regulatory documents and study reports to regulatory authorities...In-depth knowledge of clinical trial regulations (ICH/GCP),..
Postuler | Plus d'offres Senior Clinical Project Manager
Plus d'offres - Paris |
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Lieu : Paris
Société : Excelya
..and in collaboration with the other regulatory managers and administration of clinical trials:..- Fluent in English ..
Postuler | Plus d'offres Study Start Up Manager
Plus d'offres - Paris |
Lieu : Bois-Colombes Île-de-France
Société : Chiesi Group
pharmacy or other health related discipline) or equivalent.LanguagesLanguesEnglish 5 or more (1 = beginner / 6 = fluent)Technical SkillsKnowledge of principles of clinical study designKnowledge of principles of Clinical Research StatisticsKnowledge of planning tools an..
Postuler | Plus d'offres Clinical Project Manager
Plus d'offres - Bois-Colombes |
Lieu : Lyon Auverge-Rhône-Alpes
Société : Talents Solutions
Independently draft pre- and/or post-CE marking clinical investigation plans and reports...Handle statistical analysis of ongoing clinical study data...
Postuler | Plus d'offres Clinical Project Manager
Plus d'offres - Lyon |
Lieu :
Société : Chronos Consulting
The role is % remote with up to 40% travel and based in Europe.As part of the global clinical affairs team,..
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Lieu : Paris Île-de-France
Société : Pharmiweb
office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team...We provide Phase I-IV clinical development services to the biotechnology,..
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Lieu : Toulouse Occitania
Société : Pharmiweb
The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities...
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Lieu : Lyon Auverge-Rhône-Alpes
Société : Pharmiweb
We provide Phase I-IV clinical development services to the biotechnology,..and third-party vendors Provide oversight and quality control of our internal regulatory filing system Provide oversight and management of study supplies Create and maintain project timelines Coordinat..
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Lieu : Lille Hauts-de-France
Société : Pharmiweb
Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM)...
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Lieu : Bordeaux Nouvelle-Aquitaine
Société : Pharmiweb
office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team...Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM)....
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Lieu : Nice Provence-Alpes-Côte d'Azur
Société : Pharmiweb
Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management...
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Lieu : Nantes Pays de la Loire
Société : Pharmiweb
Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM)...
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Lieu : Montpellier Occitania
Société : Pharmiweb
Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM)...
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Lieu : Paris Île-de-France
Société : IQVIA
technology solutions and clinical research services to the life sciences industry...troubleshoot and influence for quality and deliveryA track record of ensuring GCP compliance and successful risk management of complex clinical studies is expectedAbility to travel as required..
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Lieu : Montpellier Occitania
Société : Pharmiweb
and final study report,..when applicable Develop operational project plans Manage risk assessment and execution Responsible for management of study vendor Manage site quality,..
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Lieu : Bordeaux Nouvelle-Aquitaine
Société : Pharmiweb
Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach...
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Lieu : Lille Hauts-de-France
Société : Pharmiweb
We provide Phase I-IV clinical development services to the biotechnology,..which includes ensuring all necessary project-specific training is provided Review and provide input for study protocol,..
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Lieu : Paris Île-de-France
Société : Pharmiweb
including direct supervision of project Clinical Research Associates and monitoring deliverables Qualifications Bachelor's degree in a health or life science-related field;..
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