Emplois actuels liés à Local Trial Manager - Paris, Île-de-France - IQVIA

  • Clinical Trial Manager

    Il y a 2 minutes


    Paris, Île-de-France ICON plc Temps plein

    Clinical Trial Manager - France - HybridICON 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 developmentWe are constantly looking for motivated, reliable and...

  • Clinical Trials Assistant

    il y a 2 semaines


    Paris, Île-de-France IQVIA Temps plein

    The IQVIA Research and Development Solutions team is focused on helping our healthcare customers to find innovative treatments solutions for patients with the common, large or rarest illnesses. Providing administrative support to the clinical teams members could make your contribution to the research. We seek dynamic and motivated people who truly want to...

  • BDM/ Solution Engineer

    il y a 5 jours


    Paris, Île-de-France Buckman International Temps plein

    DescriçãoJob Success ProfileSolution Engineer (Trial and Tissue Industry Specialist)Location:FranceLanguage(s) RequirementsFluent in English and FrenchTravel requirements70% Role summary:We are looking for a highly motivated Solution Engineer for focusing on bringing application excellence to customers in the form of trial execution and advanced attrition...

  • Clinical Project Manager

    Il y a 2 minutes


    Paris, Île-de-France Excelya Temps plein

    About the JobJoin Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.This role is an exciting opportunity to contribute to a dynamic, ambitious team in Clinical Operations. You will play a critical...

  • Clinical Research Associate

    Il y a 3 minutes


    Paris, Île-de-France R&D Partners Temps plein

    Drive the future of clinical trials as a CRA supporting a global center of excellence in high‑quality, patient‑focused research.R&D Partners is seeking a Clinical Research Associate (CRA) to support the Global Clinical Operations (GCO) Center of Excellence. This role involves conducting clinical trial activities in alignment with GCO's mission of...


  • Paris, Île-de-France Boston Scientific Temps plein

    Additional Locations:France-Auvergne-Rhône-Alpes; Belgium-Diegem; France-Bourgogne-Franche-Comté; France-Bretagne; France-Centre-Val de Loire; France-Grand Est; France-Hauts-de-France; France-Normandie; France-Nouvelle-Acquitaine; France-Occitanie; France-Pays de la Loire; France-Provence-Alpes-Côte d'Azur; France-Voisins le Bretonneux;...


  • Paris, Île-de-France bostonscientific Temps plein

    Additional Locations: France-Auvergne-Rhône-Alpes; Belgium-Diegem; France-Bourgogne-Franche-Comté; France-Bretagne; France-Centre-Val de Loire; France-Grand Est; France-Hauts-de-France; France-Normandie; France-Nouvelle-Acquitaine; France-Occitanie; France-Pays de la Loire; France-Provence-Alpes-Côte d'Azur; France-Voisins le Bretonneux;...


  • Paris, Île-de-France MSD France Temps plein

    Job DescriptionContrat de stage – merci d'indiquer sur votre CV la date et la durée de votre stage.Mission générale de la fonctionConstitution des dossiers réglementaires Essais cliniques (Demande d'Autorisation d'essais Cliniques et demande de Modifications Substantielles) pour évaluation dans le cadre du règlement (EU) No 536/2014.Suivi des...

  • R&D Project Manager

    Il y a 3 minutes


    Paris, Île-de-France DS Smith Temps plein

    About UsWe are DS Smith, together with International Paper, we are a global leader in sustainable packaging solutions and other fibre-based products. We believe a better, more sustainable tomorrow is possible with the right people, who challenge and support one another to enact positive change. We employ more than 65,000 colleagues in North America and...


  • Paris, Île-de-France MSD Temps plein

    Job DescriptionContrat de stage – merci d'indiquer sur votre CV la date et la durée de votre stage. Mission générale de la fonctionConstitution des dossiers réglementaires Essais cliniques (Demande d'Autorisation d'essais Cliniques et demande de Modifications Substantielles) pour évaluation dans le cadre du règlement (EU) No 536/2014.Suivi des...

Local Trial Manager

il y a 2 heures


Paris, Île-de-France IQVIA Temps plein

Paris, France | Full time | Home-based | R1520016Job OverviewProject Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients' lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. Clinical Project leads can run their own studies. The Project Lead focus is on leveraging therapeutic expertise and IQVIA's suite of solutions to drive operational excellence and strategic leadership with our customers.Essential Functions Participate in bid defense presentations in partnership with Business Development and may lead the presentation for smaller, less complex regional studies.May be responsible for delivery and management of smaller, less complex, regional studies.Develop integrated study management plans with the core project team.Accountable for the execution of clinical studies, or assigned portion of clinical studies, per contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.Set objectives of the core project team and/or sub-team(s) according to agreed upon contract, strategy and approach, effectively communicate and assess performance.Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.Monitor progress against contract and prepare/present project and/or sub-team information proactively to stakeholders internally and externally.Manage risk (positive and negative) and contingencies proactively and lead problem solving and resolution efforts.Achieve project quality by identifying quality risks and issues, responding to issues raised by project team and/or sub-team members and planning/implementing appropriate corrective and preventative action plans.May serve as primary or backup project contact with customer and would then own the relationship with the project's key customer contacts, as well as communicate/collaborate with IQVIA business development representatives, as necessary.;Build the cross-functional project team and lead their efforts; responsible for managing cross-collaboration of the core team and for overall project delivery to support milestone achievement and to manage study issues and obstacles.;Ensure the financial success of the project.Forecast and identify opportunities to accelerate activities to bring revenue forward.Identify changes in scope and manage change control process as necessary.Identify lessons learned and implement best practices.May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements.;Adopt corporate initiatives and changes and serve as a change advocate when necessary.Provide input to line managers of their project team members' performance relative to project tasks.Support staff development and mentor less experienced project team members on assigned projects to support their professional development.;Qualifications Hybrid role - candidate needs to attent to Paris officesBachelor's Degree Life sciences or related field Req5 years of prior relevant experience including > 1 years project management experience or equivalent combination of education, training and experience. ReqAdvanced knowledge of job area, and broad knowledge of other related job areas, typically obtained through advanced education combined with experience. ReqKnowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. Broad protocol knowledge; therapeutic knowledge desired. Good understanding of the competitive environment and how to communicate/demonstrate value through IQVIA solutions.;Communication - Strong written and verbal communication skills including good command of English language. Strong presentation skills.Problem solving - Strong problem solving skills.Leadership - Ability to work through others to deliver results to the appropriate quality and timeline metrics, monitoring/managing performance and providing feedback, experience productively partnering cross functionally and with customers to advance work effectively and efficiently.Leadership - Ability to make decisions, bringing clarity to disparate information to inform actions and drive results.Organisation - Planning, time management and prioritization skills. Ability to organize resources needed to accomplish tasks, set objectives and provide clear direction to others, experience planning activities in advance and taking account of possible changing circumstances.Prioritisation - Ability to handle conflicting priorities.Quality - Attention to detail and accuracy in work. Results-oriented approach to work towards delivery and output.Quality - Demonstrated learning agility and openness to learning and keeping own knowledge and skill set current and evolving.IT skills - Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint.Collaboration - Ability to establish and maintain effective working relationships with coworkers, managers and clients. Strong customer service skills.Cross-collaboration - Ability to work across geographies displaying high awareness and understanding of cultural differences.Finances - Good understanding of project financials including experience managing, contractual obligations and implications.IQVIA Core Competencies - Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, innovation, Ownership).IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more