iqvia Jobs

ernal Job Description IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries

IQVIA Biotech is recruiting for an experience CPM/Sr CPM to join our respected, well established team. To be considered for this role you must have a minimum of 4 years regional/global CPM experience

Job Overview Develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by

Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs)

INTSEL CHIMOS , laboratoire pharmaceutique français situé à Saint-Cloud (92) titulaire / exploitant / distributeur / dépositaire de médicaments hospitaliers et en ville ainsi qu’ importateur / distrib

Provide expert review and guidance for production of Data Management deliverables including CRF/e-CRF, database design and set-up, validation definition and programming, Data Management Plan and datab

Join IQVIA as Trainee Clinical Research Associate / Associate CRA (m/w/d) in the sponsor dedicated team and work in home-office throughout Germany. In our Clinical Functional Service Partnership model

Location: Remote, candidates should preferably be based in Spain, Portugal or Eastern Europe. Join IQVIA’s Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. We bring

RADDS Japan での募集です。 --------------------- 【部署・チーム名】 -------------- グローバルで先行していた「RADDS」（Regulatory Affairs & Drug Development Solutions）と呼ばれる新組織を日本でも始動。顧客のニーズに応じて薬事対応、開発戦略立案、臨床開発などのサービスを一体的に提供する体制を

Job Overview Under supervision, provide support enabling the accurate and timely payment administration to our network of project sites. Perform duties in accordance with IQVIA Finance Standard Operat

Join IQVIA as a Clinical Research Associate 1 or Clinical Research Associate 2 / CRA I or CRA II and work home-based throughout Germany in our single sponsor department. You will enjoy the stability a

Job Overview Provide basic and some comprehensive data management expertise to the Clinical Data Management (CDM) team to provide efficient, quality data management products that meet customer needs.

Job Overview Responsible for management and service delivery excellence for assigned projects, covering single or multiple Lifecycle Safety functions (clinical trial and / or post-market). Provide lea

The Global Study Associate Director (GSAD) is a business-critical role within Study Management, BioPharmaceuticals Clinical Operations, whose main accountability is the delivery of clinical studies. T

Job Overview This role is an individual contributor assigned to designated Delivery Unit(s), sponsor(s), business line(s), and/or specific tasks as defined by the line manager (LM). The purpose of thi

岗位职责： 1\. 进行二手数据的搜集、分析和整理，尤其是相关文献、行业信息及资讯的搜索、阅读、分析和归纳 2\. 整理一手数据，包括行业代表人物访谈纪要等，挖掘有价值的信息 3\. 协助项目组同事进行定量数据的分析，发现数字背后的规律 4\. 协助项目组同事完成最终报告的撰写，包括PPT的内容调整，版式的设计和修订，翻译等 5\. 协助完成团队交办的其他相关工作 任职要求： 1\. 全日制本科学

External Job Description Overview: The Site Investigational Product Specialist (SIPS) will serve as a subject matter expert for nursing administration as it relates to the process and procedure of the

Site Activation Manager (Global) Sponsor Facing Homebased Job Overview Lead and manage the strategic, operational, and financial delivery of Site Activation activities across assigned studies and regi

Únete a nosotros en nuestro emocionante trayecto! IQVIA ™ es The Human Data Science Company ™, enfocada en el uso de datos y ciencia para ayudar a los clientes de la salud a encontrar mejores solucion

Únete a nosotros en nuestro emocionante trayecto! IQVIA ™ es The Human Data Science Company ™, enfocada en el uso de datos y ciencia para ayudar a los clientes de la salud a encontrar mejores solucion