20 publicaciones de empleo destacadas de writer en spain (¡Están contratando!)

Principal Medical Writer - FSP
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Word
- Doctorado
- Investigación
2d
Copywriter B2B
FeverUp —Madrid, Madrid provincia
- Jornada completa
- Español
- Inglés
- Seguro dental
- Abono gimnasio
Senior External Communication Specialist
Fluidra North America —Sant Cugat del Vallès, Barcelona provincia
- Español
- Inglés
Senior Medical Writer
TFS HealthScience —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Doctorado
- Inglés
- Máster
Solicitud rápida
Head of Content
OnTheGoSystems —Barcelona, Barcelona provincia
- Jornada completa
- Teletrabajo
- Inteligencia artificial
- Marketing
Solicitud rápida
11d
Principal Product Designer
The Knot Worldwide —Barcelona, Barcelona provincia
- Trabajo híbrido
- Oficina
Content Marketing Manager (EU)
CoVet —En remoto
- Jornada completa
- Teletrabajo
- Marketing
Solicitud rápida
Executive Communications Manager EMEA, AWS Partner Organization
AWS EMEA SARL (Spain Branch) —Madrid, Madrid provincia
- Jornada completa
- Marketing
- AWS
- Grado
Staff Writer (German speaker)
FeverUp —Madrid, Madrid provincia
- Jornada completa
- Español
- Inglés
8d
Technical writer
CIMSA Ingeniería de Sistemas —Barcelona, Barcelona provincia
- Español
- Informática
- Inglés
Maintenance & Operation Tiger Technical Data
Airbus Helicopters España, SA —Albacete, Albacete provincia
- Jornada completa
- Español
- Inglés
11d
Trainee Creative Copy - Prácticas
Omnicom Health —Barcelona, Barcelona provincia
- Contrato en prácticas
Marketing Specialist Team Lead, Amazon Business
Amazon Business EU SARL, Sucursal en España —Madrid, Madrid provincia
- Jornada completa
- Marketing
- Project management
- Grado
Trainee /becario
OncologyPipeline —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Grado
Medical Advisor Oncology
OncologyPipeline —Madrid, Madrid provincia
- Media jornada
Applied Research Scientist [Machine Visibility]
saas.group —Barcelona, Barcelona provincia
- Teletrabajo
- Doctorado
- Investigación
- Máster
Solicitud rápida
Director - Global Head of Solar Research
Wood Mackenzie Inc. —Madrid, Madrid provincia
- Jornada completa
- Microsoft Excel
Solicitud rápida
14h
People Data Reporting and Visualisation Lead
Sanofi —Barcelona, Barcelona provincia
- Grado
- Recursos humanos
- Liderazgo
SRO Principal Engineer Nuclear Operations
Westinghouse Electric Company —San Sebastián de los Reyes, Madrid provincia
- Trabajo híbrido
- Inglés
- Enseñanza
- Seguro de vida
Content Strategist
Happyrobot Inc. —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Salesforce
- Marketing

Quiero recibir la alerta de empleo más reciente de writer en spain

Al iniciar sesión en tu cuenta, aceptas las Condiciones del servicio de SimplyHired, nuestra Política sobre cookies y nuestra Política de privacidad.

Principal Medical Writer - FSP

IQVIA -
Madrid, Madrid provincia

Solicitar ahora

Detalles del empleo

Jornada completa
Hace 2 días

Cualificaciones

Microsoft Word
Investigación clínica
Doctorado
Investigación
Máster
Project management
Grado
Farmacia
Gestión del tiempo

Descripción completa del empleo

Madrid, Spain | Full time | Home-based | R1523797

Overview

We are seeking an experienced Senior Medical Writer to lead the development of high-quality clinical and regulatory documents supporting global regulatory submissions. This role plays a critical part in ensuring that documents such as Investigator’s Brochures (IBs), Clinical Study Reports (CSRs), and marketing authorization applications (MAAs/NDAs/BLAs) are scientifically accurate, consistent, and aligned with program objectives and global regulatory requirements.

The successful candidate will act as a lead writer for key summary documents, providing strategic guidance to cross-functional teams while overseeing medical writing activities across multiple compounds. This position reports to the Director of Medical Writing (or above)

Key Responsibilities

Lead the development of high-quality clinical and regulatory documents (e.g., Investigator’s Brochures, Clinical Study Reports, clinical summaries, and marketing authorization submissions) in compliance with global regulatory guidelines (ICH, FDA, EMA) and internal standards
Serve as the lead writer for key summary documents, overseeing medical writing activities across multiple compounds or programs
Provide strategic guidance to cross-functional teams on document content, messaging, and regulatory positioning to ensure alignment with program goals
Manage medical writing projects, including planning, timelines, resource coordination, and delivery to ensure milestones and submission deadlines are met
Collaborate with cross-functional stakeholders (Clinical, Regulatory Affairs, Biostatistics, Safety, etc.) to gather, interpret, and accurately present clinical data
Mentor and support other medical writers, ensuring high-quality, scientifically sound, and consistent deliverables across projects
Review and edit project-related documents to ensure accuracy, clarity, consistency, and compliance with templates and style guides
Attend project and team meetings to provide expert input on document development, study data interpretation, and process improvements
Contribute to and lead process improvement initiatives to enhance efficiency, quality, and consistency in document preparation
Develop, maintain, and refine standard operating procedures (SOPs), templates, and best practices for medical writing
Stay current with evolving global regulatory requirements, industry trends, and therapeutic area knowledge to ensure compliance and innovation

Qualifications

Bachelor’s degree in a scientific, clinical, regulatory, or related field required; advanced degree (e.g., MSc, PhD, PharmD, MD) preferred
Minimum of 5+ years of experience in medical writing within the biopharmaceutical, biotechnology, or CRO industry; equivalent experience in clinical or preclinical development will also be considered
Strong knowledge of global regulatory requirements and guidelines (e.g., ICH, FDA, EMA) across all phases of clinical development
Broad understanding of clinical research processes, including study design, data analysis, and regulatory submission requirements
Demonstrated ability to lead writing activities for complex documents and provide strategic input to cross-functional teams
Excellent written and verbal communication skills, with the ability to clearly and accurately present complex scientific and clinical information
Strong organizational, time management, and project management skills, with the ability to manage multiple priorities and meet tight deadlines
Proven ability to work collaboratively in a cross-functional, team-oriented environment while also operating independently when needed
High attention to detail with a commitment to quality, consistency, and scientific accuracy
Proficiency in Microsoft Word and document formatting best practices
Experience with electronic document management systems (eDMS) and familiarity with document templates, style guides, and structured authoring tools

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.

Solicitar ahora

Refina tu búsqueda

writer empleos en spain

Principal Medical Writer - FSP

Copywriter B2B

Senior External Communication Specialist

Senior Medical Writer

Head of Content

Principal Product Designer

Content Marketing Manager (EU)

Executive Communications Manager EMEA, AWS Partner Organization

Staff Writer (German speaker)

Technical writer

Maintenance & Operation Tiger Technical Data

Trainee Creative Copy - Prácticas

Marketing Specialist Team Lead, Amazon Business

Trainee /becario

Medical Advisor Oncology

Applied Research Scientist [Machine Visibility]

Director - Global Head of Solar Research

People Data Reporting and Visualisation Lead

SRO Principal Engineer Nuclear Operations

Content Strategist

Quiero recibir la alerta de empleo más reciente de writer en spain

Related Searches

Herramientas para candidatos

Herramientas para empresas

Buscar

Mantener la conexión