6 publicaciones de empleo destacadas de clinical research en 08171 sant cugat del vallès barcelona provincia (¡Están contratando!)

Medical Safety Director, Clinical Scientist
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Doctorado
- Teletrabajo opcional
2h
Data Steward (Barcelona)
EBMT —Barcelona, Barcelona provincia
- De 31.574 € a 34.595 € al año
- Jornada completa
- Trabajo híbrido
- Inglés
- Investigación
- SQL
2h
Applied AI Consultant Engineer
Alira Health —Barcelona, Barcelona provincia
- Jornada completa
- Informática
- Máster
- SQL
Senior Software Engineer
Tempus —Barcelona, Barcelona provincia
- De 60.000 € a 80.000 € al año
- Jornada completa
- AWS
- Desarrollo de software
- Inteligencia artificial
IT Solutions Operations Engineer (Applications Support)
Eurofins —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Oracle
- SQL
- Scripting
Solicitud rápida
Senior Director - Enterprise AI Platforms
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Azure
- Informática

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Medical Safety Director, Clinical Scientist

IQVIA -
Barcelona, Barcelona provincia

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Detalles del empleo

Jornada completa
Hace 2 horas

Beneficios

Teletrabajo opcional

Cualificaciones

Doctorado
Farmacia

Descripción completa del empleo

Barcelona, Spain | Full time | Home-based | R1562155

Position Summary

The Medical Safety Director, Clinical Scientist provides clinical science support to product activities, ensuring high-quality clinical input into routine maintenance documentation, safety and labeling deliverables, and issue resolution activities.

This role partners closely with cross-functional product teams, represents Clinical Science in key governance forums, and provides expert clinical review and recommendations to support product benefit-risk evaluation, regulatory compliance, and labeling consistency. The position works in close collaboration with the Global Clinical Science Lead, escalating critical issues and contributing to timely, scientifically robust decision-making.

Key responsibilities

Participate in relevant product-team meetings including Labelling Working Group (LWG)as the Clinical Science representative
Gather and provide necessary information under guidance from the GCL
Review draft documents (PBRER/PSUR, CCDS/CCSI, US Annual Report) from a Clinical Science perspective; share key points and any critical issues with the GCL
Participate in relevant Safety Management Team (SMT) meetings as the Clinical Science representative
Review Safety Validation and Evaluation Report draft documents; share key points and any critical issues with the GCL etc.

Required Experience

MD, PharmD, PhD, or equivalent advanced life sciences degree with strong clinical science expertise and the ability to interpret clinical, safety, and scientific literature within a benefit-risk framework.
Proven experience supporting regulatory and pharmacovigilance deliverables, including PBRER/PSUR, CCDS/CCSI, US Annual Reports, and Safety Evaluation Reports.
Hands-on experience reviewing and contributing to clinical sections of safety, regulatory, and labeling documents, ensuring scientific accuracy, consistency, and compliance.
Strong knowledge of drug safety, pharmacovigilance, risk management, and global labeling processes within the pharmaceutical industry.
Experience participating in cross-functional product teams, Safety Management Teams (SMTs), and Labeling Working Groups (LWGs) as a Clinical Science representative.
Demonstrated ability to evaluate clinical and safety data, identify risks, resolve issues, and provide clear, actionable recommendations and document wording.
Experience supporting CCDS updates, emerging safety topics, issue resolution activities, and responses to regulatory or local market queries.
Excellent scientific communication, stakeholder management, and collaboration skills within a global matrix environment.
Strong attention to detail, quality mindset, and ability to manage multiple priorities while delivering high-quality outputs within tight timelines.

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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Quiero recibir la alerta de empleo más reciente de clinical research en 08171 sant cugat del vallès barcelona provincia

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