Ofertas de empleo en IQVIA

• Nivel de experiencia---
• Tipo de contratoA tiempo completo
• Publicada17 feb.

Teletrabajo Spark LESS

Use your scientific and foreign language expertise to join the world’s leading comprehensive pharmaceutical safety services organization at on a fast-growing team performing medical information call center services. Apply your knowledge and expertise, including complex decision making, to review, assess and process safety and product quality information. Be a part of a global team to help ensure the safety profiles of products marketed around the world with development opportunities to ultimately provide oversight on projects and teams.

Responsibilities

• Provide phone support to health care professionals and consumers regarding adverse events, product quality complaints, medical inquiries, product support, and other needs as required. This does NOT include commercial sales support.
• Receive, triage, review and process Lifecycle safety operational data. Perform data entry for tracking and Lifecycle safety databases, coding relevant medical terminology, writing descriptive narratives, generating queries pertinent to the case, performing quality control, assisting with reconciliation, driving case closure, coordinating translations.
• Receive and document incoming telephone calls or emails from investigative sites or other sources reporting safety data.
• Build a positive, collaborative team environment with Lifecycle safety team members, lead by example, provide training and mentoring for less experienced team members and operations staff.
• Establish and maintain effective team project service operations communications
• Liaise with Project Manager by proactively identifying issues and proposing solutions
• Participate in training across Lifecycle safety process service offerings, participate in working groups as applicable in implementation of new initiatives
  
  

Required Knowledge, Skills And Abilities

• Must be a Pharmacist.
• Excellent written and verbal skills in English (min. C1) and German language (min. C2 or native).
• Willingness and aptitude to learn new skills across our Lifecycle Safety service lines.
• Excellent attention to detail and accuracy maintaining consistently high-quality standards.
• Excellent organizational skills and time management skills.
• Ability to establish and maintain effective working relationships with coworkers, managers and clients.
• Ability to work effectively on multiple projects simultaneously, organize own workload and effectively manage competing priorities.
  
  

Minimum Required Education And Experience

• Bachelor’s Degree in Pharmacy
• Fluency in English (min. C1 level) and German language (min. C2 level or native).
  
  

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 at https://jobs.iqvia.com

At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes.

• Nivel de experiencia---
• Tipo de contratoA tiempo completo
• Publicada17 feb.

Teletrabajo Office

Senior Project Manager, eCOA

Location: UK, Spain, fully remote

We are seeking a Project Manager to manage delivery of eCOA projects to internal and external clients.

Job Overview

Validates the project scope, plans and schedules for moderately complex projects; adheres to metrics for project success and begins to suggest appropriate metrics; provides input to and applies standards (e.g. delivery process, roles and responsibilities, operational norms, compliance).

Responsibility

• Manage day to day implementation of eCOA projects
• Manage internal staff to support customer projects and manage internal service projects
• Define and monitor project scope, budget, timelines, resources, quality and deliverables for the full project life cycle
• Ensure the project team adheres to high quality service and all applicable corporate and client policies and standards
• Regularly review project contract terms and conditions, and project plan to ensure that all assumptions are still valid
• Work in close collaboration with the internal or external project stakeholders to achieve the study goals
• Establish strong customer relationships and seek opportunities to increase customer satisfaction and deepen relationships
• Communicate effectively with customers to identify needs and propose solutions
• Keep customers well informed on status of internal service efforts and serves as liaison between internal staff and customer
• Provide technical direction for the development, design, and systems integration for customer engagements
• Responsible for managing the development, review and approval of project related study documentation during throughout the full life cycle of the project implementation
• Provide regular updates and reports to Sponsor and IQVIA upper management
• Conduct regular status meetings, reviewing project schedule, risks, issues and outstanding action items
• Implement and monitor a risk management plan at the project level (raise to program level, as necessary)
• Implement corrective actions as needed to maintain project performance
• Identifies opportunities for improving and streamlining projects
• Manage vendor relationship and tasks
• Manages the Lessons Learned process throughout the project lifecycle
• Communicate customer requirements to the product management teams, advocate on the customer’s behalf, and communicate the status of enhancement requests to customers
• Manage project team members across multiple locations and time zones
• International Travel required as needed
  
  

Education, Skills And Experience Required

• Bachelor Degree or equivalent
• A thorough understanding of Project Management principles - PMP / PRINCE II certification is a plus
• In-depth project management experience ideally within clinical research
• Experience and understanding of the clinical research environment and GCP principles
• Strong leadership, diplomatic and motivational skills
• Open, transparent and excellent communication skills, fluency in English both verbal and written
• Proven ability to work creatively and analytically in a problem-solving environment
• Excellent in planning, organizing and monitoring
• Self-motivated, decisive, with the ability to adapt to change and competing demands
• Able to communicate and deal effectively with all levels of the organization Confident and comfortable with public speaking in front of a large and diversified audience. Ability to adjust presentation material for differing audience
• Solid technical background, with understanding or hands-on experience in software development and clinical technologies (EDC, eCOA, IWRS etc.)
• Strong working knowledge of Microsoft Office tools
• Eligible to live and work in the UK without VISA sponsorship
  
  

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 at https://jobs.iqvia.com

• Nivel de experiencia---
• Tipo de contratoA tiempo completo
• Publicada16 feb.

Teletrabajo Spark

JOIN OUR TEAM

This position will provide broad support on monitor and analyze the changes and evolution of the local regulatory environment, including guidance and regulations from regulatory authorities, trade organizations, working groups, and relevant industry thought leaders for both drug and medical devices. y activities and requests.

Responsibilities:

• Assess regulatory intelligence information for relevance and impact to industry’s internal processes, drug development projects and/or regulatory strategies to create and enrich the IQVIA proprietary documents.
• Monitoring agency and professional websites, local specialized press, conferences and selecting documents to be integrated in line with the IQVIA scope, editorial and intelligence management processes.
• Identify business critical aspects and communicate effectively to internal and external stakeholders. This includes regular updates on new information that could impact clinical trial execution, pharmacovigilance activities, manufacturing quality as well as other ad hoc requests.
• Synthesize information from regulatory documentation as well as interaction with local country experts as needed.
• Share/Input data into systems or tools to enable effective knowledge management of country level operational intelligence data.
• Develop and refine regulatory intelligence processes and procedures to build efficiencies.
  
  

Required Knowledge, Skills And Abilities Essential

• Proficient in proof reading and editing in Arabic / French Native speaker Languages and English
• Capability to work remotely with peers in an international environment.
• Good understanding of the drug development and commercialization process
• Ability to research, analyze and extrapolate critical regulatory information.
• Highly organized and able to work independently to meet deliverable on time and on target.
• Team-oriented and strong relationship builder, ability to effectively collaborate with a range of individuals across the organization and externally.
• Attentive to details and focused on quality output.
• Effective communicator - - both written and oral - in a multi-discipline team environment
• Proficient in the navigation of intelligence database(s)
  
  

IQVIA™ is an equal opportunity employer. We make employment decisions based on qualifications and merit. We prohibit discrimination based on any unlawful consideration such as age, race, national origin, gender or other "protected status.“

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 at https://jobs.iqvia.com.

At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes.

• Nivel de experiencia---
• Tipo de contratoA tiempo completo
• Publicada16 feb.

Teletrabajo Excel Spark Office Word

IQVIA is seeking a Project Support Coordinator, to provide administrative support to the field based staff of complex multiple projects, and helping with the smooth running of day to day activities for the team. This will be a varied and busy role, where strong administrative experience, excellent communication skills and ability to work autonomously are essential.

The successful candidate will be an effective communicator with an excellent telephone manner, ideally with experience of working within a support / call centre role who can demonstrate strong IT/data skills, strong time management skills and is proficient with MS Office packages and ideally CRM knowledge.

Responsibilities

• To work collaboratively across the Team Coordinator function, and understand how the function contributes to the Commercial business.
• To be the first point of contact for all queries relating to the project, handling and addressing issues where appropriate, or else directing queries to the most appropriate contact.
• To follow processes and procedures (new employee, leaver, transfer) and work with departments (HR, Fleet, Resourcing, HR-PSC, Amex, BT etc.) to ensure effective team administration. Ensure that systems are updated accordingly.
• To track levels of absence, identify sickness trends within the project and highlight cost implications as appropriate.
• To facilitate production and documentation of presentations and organize team/customer meetings, finalizing minutes in collaboration with Project Director
• To support Month end administration, ensuring daily rates are allocated to field teams along with relevant time sheet, accurately collate information in connection with the Rolling Forecast, within project deadlines. To conduct financial tracking for project revenue recognition and liaising with Management Accounts.
• To undertake diary management of Project Director.
  
  

Skills And Qualifications

• Good verbal and written communication skills, telephone manner, team working skills, flexible attitude to work
• Good prioritization skills
• Fluency in English
• Able to use initiative, plan ahead, proactive in problem solving, diplomatic and able to demonstrate appropriate decisions within scope of authority
• Able to share experience and learning, able to priorities and liaise with field staff and customers effectively
• Intermediate understanding of Word, Power point and basic Excel
• Ability to establish and maintain effective working relationships with co-workers, managers and clients.
• Eligibility to work full-time in the EU
  
  

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, colour, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

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 at https://jobs.iqvia.com.

At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes.

• Flexibilidad horariaSí
• Nivel de experiencia---
• Tipo de contratoA tiempo completo
• Publicada13 feb.

¿Tienes experiencia como técnico/a de control de calidad? ¿Quieres trabajar en una empresa multinacional líder en agricultura sostenible y gestión eficiente del agua? ¡Únete al equipo de Industrias Químicas del Vallés!

Esta es una gran oportunidad para crecer a nivel profesional en un sector en auge y en una empresa sólida y comprometida con la sostenibilidad social, económica y medioambiental.

Quiénes somos:

Como líder mundial en sanidad vegetal basada en sales de cobre, desde hace más de 80 años en IQV ofrecemos a los agricultores las soluciones más eficaces y sostenibles para proteger sus cultivos.

La empresa forma parte del grupo MAT Holding, cuyo propósito es cuidar la agricultura y el agua mediante soluciones que fomentan la sostenibilidad, la eficiencia y la rentabilidad de la gestión agrícola e hídrica.

Para más información, visita www.iqvagro.com

Cuál será tu misión:

Integrado/a en el equipo de laboratorio y reportando a la Responsable de Laboratorio, tu misión principal será: Controlar la calidad de producto, packaging y contaminación cruzada, cumpliendo los plazos, realizando una gestión eficaz y eficiente y fomentando el trabajo en equipo.

Cómo será tu día a día:

Tus funciones principales serán:

• Control de Calidad de Producción y Recepción de Materias Primas según Planes de Control de Calidad existentes.

• Control de Contaminación cruzada de las limpiezas y productos de formulación y envasado según Plan de Control.

• Desarrollo y validación de métodos analíticos

• Ejecución de los análisis necesarios para los estudios BPL: Cobre, pH, Tamaño de partícula, % Activo HPLC, etc.

• Colaborar en la Implementación y mantenimiento de la ISO17025 (validación de métodos, mantenimiento de la documentación…)

• Calibración y verificación de Equipos de Laboratorio.

Qué buscamos en ti:

-Formación grado universitario en Química

-Pasión por el control de calidad

-Ganas de aprender y colaborar

-Habilidades para manejar equipos de laboratorio

-Experiencia en entornos laboratorio entre 1 a 3 años

-Conocimientos en BPL y/o ISO17025 será un plus

Qué ofrecemos:

Esta es una gran oportunidad profesional para incorporarte a una empresa multinacional sólida e innovadora líder en su sector, con buen ambiente de trabajo y un equipo altamente competitivo, y posibilidades reales de crecer a nivel profesional.

Ofrecemos posición indefinida a tiempo completo y jornada partida.

Además, también disfrutarás de:

• Horario flexible

• Jornada continuada en agosto

• Descuentos y ventajas exclusivas en primeras marcas, viajes y espectáculos

🌾🚜¡Únete al equipo IQV, ayúdanos a mejorar la agricultura!