20 publicaciones de empleo destacadas de medical writing en barcelona, ct (¡Están contratando!)

MEDICAL WRITING SENIOR MANAGER
Almirall —Sant Feliu de Llobregat, Barcelona provincia
- Jornada completa
- Doctorado
- Inglés
- Máster
Associate Principal/Principal Qualitative Research, Patient Centered Solutions
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Teletrabajo
- Doctorado
- Inglés
- Investigación
Senior Medical Writer - FSP
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Word
- Doctorado
- Investigación
- Teletrabajo opcional
Medical Writer Supervisor
Remedy Edge Spain —Barcelona, Barcelona provincia
- Español
- Doctorado
- Inglés
Solicitud rápida
Expert Medical Regulatory Writer
Sanofi —Barcelona, Barcelona provincia
- De 60.000 € a 80.000 € al año
- Doctorado
- Inglés
- Máster
MEDICAL AFFAIRS SENIOR MANAGER Temporary
Almirall —Barcelona, Barcelona provincia
- Jornada completa
- Doctorado
- Inglés
- Investigación
Medical Information Manager
LEO Pharma A/S —Barcelona, Barcelona provincia
- Español
- Enfermería
- Habilidades de comunicación
Associate Director, IMACE Scientific Content, NS
Novartis —Barcelona, Barcelona provincia
- De 73.100 € a 135.700 € al año
- Jornada completa
- Doctorado
- Inglés
- Liderazgo
6d
Associate Principal - Mixed Methods Research: Patient Experience - Home-based/Hybrid
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Doctorado
- Inglés
- Investigación
Manual QA Tester
CREALOGIX —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Español
- Inglés
- JavaScript
Solicitud rápida
Digital Lead for Medical, Regulatory Affairs & Pharmacovigilance Platforms
Opella Healthcare Group —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Inglés
- Máster
MEDICAL AFFAIRS SENIOR MANAGER
Almirall —Barcelona, Barcelona provincia
- Jornada completa
- Doctorado
- Inglés
- Investigación
Front Desk Hospitality Agent
Sonder Holdings —Barcelona, Barcelona provincia
- Disponibilidad fin de semana
- Inglés
- Hotel
- Recepción
- Seguro dental
- Seguro oftalmológico
Business Development Manager – Medical Affairs Solutions (IQVIA Pharma Review)
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Desarrollo de negocios
Promotional Regulatory Affairs Specialist, Europe
Alcon —Cornellà de Llobregat, Barcelona provincia
- Jornada completa
- Español
- Inglés
- Grado
9d
Epidemiologist (real world country operations)
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
HTA & Modelling Science Lead
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Oficina
- Grado
Associate Principal / Principal, Clinical Outcome Assessment (COA) Strategy Consulting
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Doctorado
- Investigación
- Máster
Global Head, RWE Biostatistics
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Investigación
- Máster
- Grado
- Teletrabajo opcional
1d
Manager Risk Management
Novartis —Barcelona, Barcelona provincia
- De 46.300 € a 86.100 € al año
- Jornada completa
- Doctorado
- Inglés
- Máster
21h

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MEDICAL WRITING SENIOR MANAGER

Almirall -
Sant Feliu de Llobregat, Barcelona provincia

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Detalles del empleo

Jornada completa

Cualificaciones

Doctorado
Inglés
Máster
Farmacia

Descripción completa del empleo

The Medical Writing Senior Manager is responsible for leading the development, coordination, and delivery of high‑quality clinical and regulatory documents that support Almirall’s R&D programs. This role ensures scientific accuracy, regulatory compliance, and alignment with strategic and global submission objectives across therapeutic areas. The position collaborates cross‑functionally with clinical development, regulatory affairs, patient safety, biostatistics, and external partners to ensure timely, efficient, and effective communication of scientific data. The role also drives innovation through the informed use of AI/GenAI technologies and strengthened process governance with external vendors.

CORE RESPONSIBILITIES

Clinical & Regulatory document writing leadership

Lead the planning, writing, and review of clinical and regulatory documents including protocols, investigator brochures, clinical study reports, paediatric documentation, responses to HA questions, and submission dossiers.
Ensure consistency, clarity, and scientific integrity across all documents in compliance with ICH guidelines, GCP, and global regulatory requirements.

Cross‑functional collaboration & writing strategic Input

Work closely with cross‑functional teams to gather scientific input and ensure alignment on messaging and content.
Provide strategic input into document planning, dossier strategy, and global regulatory submission planning.

Quality, standards & team guidance

Review and edit documents prepared internally or by external vendors to ensure scientific accuracy and adherence to standards.
Contribute to the development and maintenance of medical writing standards, templates, guidance documents, and SOPs.
Mentor and guide junior medical writers, fostering capability development and high‑quality output.

AI/GenAI‑Enabled Medical Writing excellence

Evaluate and implement AI/GenAI‑enabled authoring tools to enhance efficiency, consistency, and document quality.
Establish guardrails, quality controls, and best practices for safe, compliant, and high‑quality use of AI‑generated content.
Support change‑management activities, internal training, and workflow integration of AI/GenAI capabilities within the medical writing team.

Vendor and process governance

Manage external medical writing vendors, including selection, contracting, oversight, and performance review.
Ensure robust process governance, quality standards, and clear communication channels with external partners.

REQUIRED EDUCATION AND EXPERIENCE

Advanced degree in Life Sciences (PhD, PharmD, MD, MSc or equivalent experience).
Minimum 8 years of experience in medical writing within the pharmaceutical or biotech industry.
Proven track record in authoring and managing clinical and regulatory documents for global submissions.
Experience working with external vendors and overseeing outsourced activities.
Fluent in English.

PREFERRED SKILLS AND COMPETENCIES

Strong understanding of ICH guidelines, GCP, CTD requirements, and global regulatory frameworks.
Knowledge of AI/GenAI tools and practical experience integrating them into document workflows is highly desirable.
Proficiency with document management systems, authoring tools, and structured content management approaches.
Strong communication skills and ability to work in dynamic cross‑functional environments.
Excellent attention to detail, strategic thinking, and ability to manage multiple priorities.
Strong influencing capacities, and vendor‑management capabilities.

Why work with Almirall?

We are a people-centric company where employees are at their best, patients and customer are at the heart of every decision, and our focus and agility allow us to deliver greater impact for all.

Additionally, for the 17th year in a row, we have been certified as Top Employer Spain, and also Top Employer Germany for the first time.

This strengthens our commitment to create a unique work environment that helps our employees to develop their skills to fullest and grow both professionally and as individuals.

We are delighted to have a great team that is proactive, innovative, and eager to transform the world of people with skin conditions.

We are proud of each one of our employees , their development, and growth: they are the success of the company.

Our purpose

"Transform the patients' world by helping them realize their hopes & dreams for a healthy life".

Our values

Care: we listen & empathize, we value diverse perspectives & backgrounds and we help each other succeed.
Courage: we challenge the status quo, we take full ownership and we learn from our success & failures.
Innovation: we put the patient and customer at the center, we create novel solutions and we empower entrepreneurial mindsets.
Simplicity: we act decisively and avoid over-analysis, we understand why before we act and we are agile & keep things simple.

At Almirall, it’s all about people!

#wearealmirall

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Refina tu búsqueda

medical writing empleos en barcelona, ct

MEDICAL WRITING SENIOR MANAGER

Associate Principal/Principal Qualitative Research, Patient Centered Solutions

Senior Medical Writer - FSP

Medical Writer Supervisor

Expert Medical Regulatory Writer

MEDICAL AFFAIRS SENIOR MANAGER Temporary

Medical Information Manager

Associate Director, IMACE Scientific Content, NS

Associate Principal - Mixed Methods Research: Patient Experience - Home-based/Hybrid

Manual QA Tester

Digital Lead for Medical, Regulatory Affairs & Pharmacovigilance Platforms

MEDICAL AFFAIRS SENIOR MANAGER

Front Desk Hospitality Agent

Business Development Manager – Medical Affairs Solutions (IQVIA Pharma Review)

Promotional Regulatory Affairs Specialist, Europe

Epidemiologist (real world country operations)

HTA & Modelling Science Lead

Associate Principal / Principal, Clinical Outcome Assessment (COA) Strategy Consulting

Global Head, RWE Biostatistics

Manager Risk Management

Quiero recibir la alerta de empleo más reciente de medical writing en barcelona, ct

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