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Pour tre ligible ce poste, vous devez rsider dans le mme pays o se trouve le poste.Tous les domaines thrapeutiquesVotre objectif principal sera de favoriser lexcellence oprationnelle et le leadership stratgique auprs de nos fournisseurs tiers et de nos clients, ainsi que de mener vos propres petites tudes, dans le cadre de votre dveloppement.Il sagit dun rle important et de haut niveau au sein de notre organisation doprations cliniques de recherche et dveloppement. La taille et lempreinte mondiale dIQVIA vous offriront ltendue des opportunits ncessaires pour dvelopper votre carrire.* Contribuer aux plans de gestion intgrs de ltude avec lquipe principale et/ou la sous-quipe du projet et assurer lutilisation cohrente des outils dtude, du matriel de formation et le respect des processus, politiques et procdures standard.* Collaborer avec dautres groupes fonctionnels au sein de lentreprise, si ncessaire, pour soutenir la ralisation des tapes cls et grer les problmes et les obstacles lis ltude.* Diriger les efforts dune sous-quipe de projet, assumer la responsabilit de la gestion de la collaboration croise de la sous-quipe pour soutenir la ralisation des jalons et grer les problmes et les obstacles.* Le cas chant, en tant que gestionnaire des fournisseurs dun projet:* laborer le plan de gestion des fournisseurs au niveau de ltude, y compris les produits livrables et les tapes, les accords sur les niveaux de service (ANS) et les rapports, le plan de communication et de remonte des problmes, la gestion des risques, le plan de classement (dossier lectronique permanent de lessai, eTMF), la stratgie de fourniture dquipements, la formation des fournisseurs, le plan de transition des membres cls de lquipe, laccs au systme.* Servir de contact principal avec le client pour les progrs, la gestion des risques et la gouvernance des fournisseurs tiers.* Grer et suivre les performances des fournisseurs par le biais dindicateurs cls de performance, de livrables et de jalons et prparer/prsenter de manire proactive ltat/les performances des fournisseurs tiers aux parties prenantes internes.* Sassurer que le budget de ltude ralise par les fournisseurs tiers est gr de manire proactive, y compris les changements de porte, et que les systmes financiers sont prcis.o Fixer les objectifs des sous-quipes du projet, conformment au contrat, la stratgie et lapproche convenus, communiquer et valuer efficacement les performances.o Surveiller les progrs par rapport au contrat et prparer/prsenter les informations sur le projet et/ou sur la sous-quipe de manire proactive aux parties prenantes internes.***To be eligible for this position, you must reside in the same country where the job is located.*****Job Overview** Associate Project 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 Associate Project Lead is a 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. The Associate Project Lead support the efforts of CPM to drive operational excellence and strategic leadership with our customers. Associate Project Leads may run their own studies, as part of their development.**Essential Functions** Provide input in to the development of integrated study management plans with the core project team and/or sub-team. Accountable for assigned portion of clinical studies as per the 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 project 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 internal stakeholders. Support the project leader to prepare/present project and/or sub-team information proactively to external stakeholders. Identify risk (positive and negative) and contingencies and partner with project leader in problem solving and resolution efforts. Achieve project quality by identifying quality risks and issues, responding to issues raised by project sub-team members and partner with project leader planning/implementing appropriate corrective and preventative action plans. May serve as primary (for small projects) or back-up project contact with customer. Lead the efforts of a project sub-team, responsible for managing cross-collaboration of the sub-team to support milestone achievement and to manage issues and obstacles. Support the project leader in ensuring the financial success of the project. Forecast and identify opportunities to accelerate activities to bring revenue forward in partnership with the senior project leader. Identify changes in scope and partner with project leader to 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**Qualifications** Associate's Degree In life sciences or related field required Req Or Bachelor's Degree In life sciences or related field required Req 2 years clinical research experience. Req Requires intermediate level knowledge of principles, theories, and concepts of a job area, typically obtained through advanced education combined with experience.; Req Knowledge 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.; Communication - Strong written and verbal communication skills including good command of English language. Strong presentation skills. Problem solving - Strong problem solving skills. 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. 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.**Chef de projet clinique associ** Le chef de projet clinique associ est un membre de lquipe de projet principale responsable de la ralisation des tudes cliniques afin de rpondre aux exigences contractuelles conformment aux PON, aux politiques et aux pratiques. Le Projet Leadership dIQVIA est une quipe mondiale de professionnels ddis au partenariat avec nos clients pour faire avancer les soins de sant #J-18808-Ljbffr