20 publicaciones de empleo destacadas de clinical research en barcelona, ct (¡Están contratando!)

Senior Medical Writer
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Doctorado
- Máster
- Grado
- Teletrabajo opcional
Medical Safety Lead - CRM
Novartis —Barcelona, Barcelona provincia
- De 69.000 € a 128.100 € al año
- Jornada completa
- Enfermería
- Inglés
- Inteligencia artificial
1d
RESOLUCIONES DE CONVOCATORIAS 2025
IGTP —Badalona, Barcelona provincia
- Jornada completa
- Enfermería
- Doctorado
- Hospital
- Oportunidades de crecimiento y desarrollo profesional
Solicitud rápida
Data Science Consultant, Discovery & Translational Science
Clarivate —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Doctorado
- Inglés
Senior Director, Drug Development
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Excel
- Investigación
- Teletrabajo opcional
Global Program Safety Lead - CRM
Novartis —Barcelona, Barcelona provincia
- De 85.100 € a 158.100 € al año
- Jornada completa
- CRM software
- Doctorado
- Inglés
1d
Senior Statistician
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Doctorado
- Inglés
Data Steward (Barcelona)
EBMT —Barcelona, Barcelona provincia
- De 31.574 € a 34.595 € al año
- Jornada completa
- Trabajo híbrido
- Inglés
- Investigación
- SQL
15h
Senior Demand Planning, Staff Analyst
Beckman Coulter Diagnostics —Barcelona, Barcelona provincia
- Jornada completa
- Inglés
- Oficina
- Máster
- Vacaciones pagadas
Associate Manager – Global Pricing (HTA and Pricing Reporting)
Sanofi —Barcelona, Barcelona provincia
- De 48.000 € a 64.000 € al año
- Jornada completa
- Microsoft Powerpoint
- Microsoft Excel
- Inglés
AI Officer - Scientific AI Harnesses, Agents & Tooling (ref. AD/26/11)
IRB Barcelona —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Informática
- Inglés
Scientific Computing Officer — HPC Systems & Performance (ref. AD/26/09)
IRB Barcelona —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Inglés
- C++
Precision Medicine Director
Novartis —Barcelona, Barcelona provincia
- De 85.100 € a 158.100 € al año
- Jornada completa
- Trabajo híbrido
- Investigación
- Liderazgo
- Plan de pensiones
RESOLUCIONES DE CONVOCATORIAS 2026
IGTP —Badalona, Barcelona provincia
- Jornada completa
- Enfermería
- Doctorado
- Hospital
- Seguro oftalmológico
- Oportunidades de crecimiento y desarrollo profesional
Solicitud rápida
Associate Director, Process & Documentation, Clinial Data Management
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Investigación
- Grado
1d
Senior Business Intelligence & Data Analyst
Beckman Coulter Diagnostics —l'Hospitalet de Llobregat, Barcelona provincia
- Jornada completa
- CRM software
- Informática
- Ventas
- Vacaciones pagadas
Global Trial Delivery Lead - Sponsor Dedicated
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Inglés
- Investigación
- Máster
- Teletrabajo opcional
Junior Research Engineer for Generative AI in Biomedicine (RE1)
Barcelona Supercomputing Center (BSC) —Barcelona, Barcelona provincia
- Jornada completa
- Informática
- Inglés
- Investigación
3d
Site Identification Lead, IQVIA Biotech
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Inglés
- Investigación
- Project management
- Teletrabajo opcional
2d
Pre-Award Grants Officer (Ref. AD/26/06)
IRB Barcelona —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Doctorado
- Sistemas ERP

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Senior Medical Writer

IQVIA -
Barcelona, Barcelona provincia

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Detalles del empleo

Jornada completa

Beneficios

Teletrabajo opcional

Cualificaciones

Doctorado
Máster
Grado
Habilidades de comunicación
Negociación

Descripción completa del empleo

Barcelona, Spain | Full time | Home-based | R1554306

Job Overview
Acts as Lead Medical Writer on most types of writing projects. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines. Performs Senior Review of straightforward medical writing deliverables. Negotiates timelines and discusses/resolves customer comments.
Provides written and verbal feedback to junior staff, and to customers when appropriate.
Keeps abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical Practice (GCP), along with developments and advances in drug development/medical and/or technical writing.

Essential Functions

Take a leading role in preparing assigned documents, including, but not limited to, confirming the scope of the task, confirming templates and specifications, negotiating and adhering to timelines, organizing document reviews, communicating directly with the customer.
Plan and organize workload for assigned projects and tasks: identify project needs, track timelines and implement customer requests.
Lead meetings on more challenging topics independently.
May present on standard Medical Writing processes at full-service bid defense meetings.
Assist in the training and development of junior staff, either formally as an assigned mentor or ad hoc for local colleagues or others. May develop and deliver training to the global team on a topic he/she has specific expertise in. May input into and deliver presentations on Medical Writing to other IQVIA groups.
May act as Project Manager for a more complex but single Medical Writing project which includes Project Finance/Invoicing responsibilities.
Complete project finance activities, including monitoring and forecasting budgeted hours.
Propose, review and approve budgets and costings for routine projects, including estimation of hours needed for Medical Writing tasks.
May take on a small customer lead role or assist an established partnership lead in their role.
May represent region or site on a Medical Writing initiative or cross-functional initiative.
Facilitates and brainstorms the identification of new ideas. May represent Medical Writing at a general capabilities audit.

Qualifications

Bachelor's Degree Bachelor's Degree in life sciences related discipline or related field
Master's Degree Master's Degree in life sciences related discipline or related field
Ph.D. Ph.D. in life sciences related discipline or related field
Typically requires at least 3 years of highly relevant experience and related competency levels.
In-depth knowledge of the structural and content requirements of clinical study reports, protocols, and similar documents and ability to identify deficiencies, errors, and inconsistencies in a protocol or report.
Good understanding of common statistical methods used in clinical trials and/or interpretation of their results.
Ability to effectively review a statistical analysis plan and to identify deficiencies, errors, and inconsistencies in statistical output
Ability to integrate, interpret, and summarize data from a variety of sources in a clear and concise manner.
Significant experience as a lead writer in preparing CSRs and protocols, with consistently positive feedback from customers and colleagues.
In depth knowledge of drug development, medical writing, and associated regulations. Good understanding of statistical principles and of medical terminology across a range of therapeutic areas.
Excellent written and oral communication skills including grammatical/technical writing skills.
Excellent attention to detail and accuracy.
Confident and effective communication and negotiation skills with customers and project managers.
Able to deliver difficult messages in constructive manner.
Demonstrates initiative and sound judgement when faced with less familiar project/document situations or challenges.
Demonstrated abilities in collaboration with others and independent thought.
Demonstrates confidence and maturity in most routine medical writing situations.
Demonstrates good judgement in requesting input from senior staff.
Ability to establish and maintain effective working relationships with coworkers, managers and customers.
Ability to effectively manage multiple tasks and projects.
Ability to proactively evaluate risks and potential issues and seek solutions and discuss appropriately with colleagues and customers.
Must be computer literate.

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

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

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clinical research empleos en barcelona, ct

Senior Medical Writer

Medical Safety Lead - CRM

RESOLUCIONES DE CONVOCATORIAS 2025

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Senior Director, Drug Development

Global Program Safety Lead - CRM

Senior Statistician

Data Steward (Barcelona)

Senior Demand Planning, Staff Analyst

Associate Manager – Global Pricing (HTA and Pricing Reporting)

AI Officer - Scientific AI Harnesses, Agents & Tooling (ref. AD/26/11)

Scientific Computing Officer — HPC Systems & Performance (ref. AD/26/09)

Precision Medicine Director

RESOLUCIONES DE CONVOCATORIAS 2026

Associate Director, Process & Documentation, Clinial Data Management

Senior Business Intelligence & Data Analyst

Global Trial Delivery Lead - Sponsor Dedicated

Junior Research Engineer for Generative AI in Biomedicine (RE1)

Site Identification Lead, IQVIA Biotech

Pre-Award Grants Officer (Ref. AD/26/06)

Quiero recibir la alerta de empleo más reciente de clinical research en barcelona, ct

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