Job Overview Review, assess, and process safety data and information across service lines, received from various sources. Distribute reports/data to both internal and external third parties following applicable regulations, Standard Operating Procedures (SOPs), and internal guidelines
Job Overview Review, assess, and process safety data and information across service lines, received from various sources. Distribute reports/data to both internal and external third parties following applicable regulations, Standard Operating Procedures (SOPs), and internal guidelines
Join our Lifecycle Safety Call Center as a Medical Information Specialist in Pharmacovigilance. This role involves making calls and requires fluency in Spanish, English, and French. You will review, assess, and process safety data and information
Job Overview Under general direction, manage all laboratory aspects of assigned clinical trial projects for a customer or a specific program for a customer. May have responsibility for a specific Customer, drug program, indication or drug
Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions Assist Clinical Research Associates (CRAs) and
Job Overview Under direct supervision, sets up studies and data integrations within sample tracking software systems, interfacing with internal and external stakeholders. Trains and assists end users with system usage. Performs system configuration and/or testing of
Overview Provides support for the activities conducted by the RA Lead, RA Labeling Lead and GLLs (Global Labelling Leads). Responsibilities • Ensures RIM systems are up-to-date with regard to Labeling CCDS events including creation of Global
Medical Science Liaison Job description: Funciones Impulsar el acceso a los productos de la franquicia para pacientes Desarrollar y mantener excelentes relaciones de trabajo con todos los clientes/partes interesadas clave, incluidos genetistas, pediatras, grupos de defensa
Job Overview Review, assess, and process safety data and information received from various sources. Distribute reports/data to internal and external third parties following applicable regulations, Standard Operating Procedures (SOPs), and internal guidelines under the guidance and
Job Overview Provide support to the Project Manager and related team members by performing routine procedures and tasks associated with the day to day running of projects throughout the entire study lifecycle (e.g. start-up, maintenance and
Essential Functions • Conduct monthly review and analysis of assigned projects, including review of revenue recognition, project performance variances, and unbilled/unearned positions. Monitor monthly compliance reports, to ensure timely reporting of revenue and billing deliverables by
IQVIA es The Human Data Science Company enfocada en utilizar la información y la ciencia para ayudar a los clientes del cuidado de la salud a encontrar mejores soluciones para sus pacientes. IQVIA ofrece un amplio
Job Overview Responsible for providing input into the generation of the study strategies and collaborating with other involved IQVIA teams. Perform, manage and co-ordinate activities for assigned opportunities and projects. Perform data mining and analysis, formulate
Orientamos la búsqueda a profesionales o estudiantes avanzados con interés en desarrollarse en áreas de soporte de negocios vinculados a la industria farmacéutica. Sus principales responsabilidades serán: Elaboración de reportes del área. Elaboración de presentaciones comerciales
Review, assess, and process safety data and information from various sources. Distribute reports/data to internal and external third parties following applicable regulations, Standard Operating Procedures (SOPs), and internal guidelines with support from senior team members. Essential
Clinical Science Associate (CSA) Launches Ubicación: Buenos Aires con disponibilidad para viajar a otras provincias del interior del país (realización de giras periódicas) Acerca del trabajo Somos una empresa de atención sanitaria innovadora e internacional comprometida
Job Overview Supervise and manage an assigned team of CPC/ PMA and their subsidiaries, who manage or support project management activities to mitigate risk, control cost, project schedule and ensure quality, time and budget deliverables are
Job Overview The role involves working directly with clients to provide strategic input, develop business opportunities, and deliver high-quality projects. The focus is on ensuring client satisfaction and meeting revenue targets, often within a specific Center
Sr. Local Trial Manager – Sponsor Dedicated. Local Trial Management services provide local management of a clinical trial (s) (or Medical Affairs data generation activity) in a country or countries. Services/deliverables include operational oversight of assigned
Are you interested in being part of a global remote monitoring team? Dont miss this opportunity where you can join our team with trainings to develop yourself as a remote monitor! Job Overview A Central Monitor
