Emplois actuels liés à Senior Clinical Project Manager - France - TRIUM Clinical Consulting NV
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Senior Clinical Research Associate
il y a 3 semaines
France, Homeworking ICON Strategic Solutions Temps pleinJoin ICON plc as a Clinical Research Associate (CRA) in Paris/Ile-de-FranceICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we drive clinical research forward by providing outsourced services to pharmaceutical, biotechnology, medical device, and public health organizations. With patients at...
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Clinical Research Associate
il y a 2 jours
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Clinical Trial Liaison
il y a 4 semaines
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Clinical Trial Liaison
il y a 4 semaines
France The Medical Affairs Company (TMAC) Temps pleinSupporting 13 sites in Germany and France Serving as a field resource for The Medical Affairs Company (TMAC), will represent the Company’s Neurology Clinical Development program. The CTL will work full time to educate, analyze, and resolve issues with clinical research sites and investigators to support efforts to improve recruitment and activation...
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GAIN Clinical specialist
il y a 4 semaines
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Business Project Manager
il y a 2 jours
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Senior Manager
il y a 8 heures
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Senior Developer
il y a 4 semaines
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Product / Project Manager (m/f/d)
il y a 2 jours
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Senior Manager, Data Analysis and Operations, Europe
il y a 2 jours
remote, france BeiGene Temps pleinBeiGene, Ltd. has proposed to change its name to BeOne Medicines Ltd. The new name is subject to shareholder approval and, once approved, use of the name will be phased in over 2025. There may be instances where "BeiGene" or "BeOne" are used to describe the company during this transition period. BeOne continues to grow at a rapid pace with challenging and...
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Senior Director, Professional Services
il y a 2 jours
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offre d'emploi, auvergne-rhone-alpes, france Acendre Temps pleinJob closes 23/3/2025About the DepartmentThe Department of Industry, Science and Resources and our broader portfolio are integral to the Australian Government's economic agenda. Our purpose is to help the government build a better future for all Australians through enabling a productive, resilient and sustainable economy, enriched by science and technology....
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Contract Manager Secteur Energie Guyane H/F
il y a 8 heures
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Digital Project Manager Website
il y a 20 heures
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Senior Market Access
il y a 2 jours
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Senior Digital
il y a 3 semaines
Roissy-en-France, Val-d'Oise Snipe RH Temps pleinSnipe RH est un cabinet de recrutement spécialisé sur les postes à caractère stratégique. Nous recherchons pour notre client, groupe industriel International spécialisé dans la fourniture et la maintenance d'équipements aéronautiques connaissant une croissance exponentielle: Un(e) senior Digital Project Manager H/F Rattaché(e) au directeur de la...
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chef de project forecasting
il y a 2 jours
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Senior Account Manager
il y a 4 semaines
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cra ii
il y a 4 semaines
France, Homeworking ICON Strategic Solutions Temps pleinWe are always on the lookout for motivated, reliable, and dedicated CRAs with at least 12 months of independent external monitoring experience on commercial studies (or a mix of commercial clinical trials), ideally in Oncology and Hematology. Experience in other therapeutic areas is also valued, especially if gained in Phase I - III commercial trials.As a...
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CRA II 24h Restantes
il y a 3 semaines
France, Homeworking ICON Strategic Solutions Temps pleinICON 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 Clinical Research Associate you will be joining the world's largest & most comprehensive...
Senior Clinical Project Manager
il y a 1 mois
Do you get energy from coordinating dynamic clinical trials with a quality-driven and pragmatic approach? The Clinical Project Manager is responsible for site and project management related to clinical trials, ensuring that milestones, timelines, budget and quality of such trials, as outlined by the study protocol, monitoring plan, SOPs, and applicable regulations and policies are met.Ensures that the rights and well-being of subjects are protected, that the reported study data are accurate, complete, and verifiable from source documents, and that the study is conducted in accordance with protocol, standard operating procedures, ISO/GCP and other applicable regulatory requirements.Is responsible for the overall documentation and adequacy of conduct, data quality, compliance and adherence to timelines for their assigned trial(s).Oversees quality of data collection, management of study supplies and resources in adherence with the project timelines, budget and quality standardsOversees start-up, enrollment, follow up and closure of clinical trial activitiesDevelops clinical study protocols and reviews/approves supporting documentation (such as monitoring plan, study plan, data management plan etc.)Develops patient recruitment and retention plansReports and presents to core teams and upper managementDevelops solutions to a variety of complex problems of diverse scope and complexity where analysis of data requires evaluation of identifiable factors.Establishes and cultivates a wide range of business relationships to facilitate completion of assignmentsInteracts with and manages vendors and stakeholders, as requiredDetermines goals and objectives for projectsLeads projects within the function or department and/or represents a specialized field in larger project teams. Influences middle management on business solutions.Represents the organization as a prime contact on contracts or projects. Interacts with senior internal management and external personnel on significant matters often requiring coordination between involved team members and stakeholders.Escalates serious issues to management.Master degree in biological or (para-) medical sciences or equivalent by experienceMinimum of 7 years’ experience in clinical research or equivalent by education or relevant experienceMinimum of 2 years’ experience as Clinical Project Leader and previous experience as a CRA is a plusStrong experience using Microsoft applications (Excel, Word, PowerPoint, Outlook)Excellent oral and written communications skillsExcellent interpersonal skillsTeam playerInspirational and motivational skillsDemonstrates ability to manage and oversee projects and related team activitiesDemonstrates ability to make timely and well-reasoned decisionsDemonstrates ability to effectively and persuasively communicate verbally and in writingDemonstrates ability to identify and adapt to shifting priorities and competing demandsAbility to maintain composure in difficult circumstancesSensitive to cultural differencesFluent in Dutch, French and English. QbD Group offers you an attractive and competitive salary package, that will be tailored to individual needs, considering legal requirements and local laws and regulations.