20 publicaciones de empleo destacadas de clinical research en tres cantos, md (¡Están contratando!)

Director, Medical Safety
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- Jornada completa
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- 41.000 € al año
- Jornada completa
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Manager –Global Advisory Services
IQVIA —Madrid, Madrid provincia
- Jornada completa
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- Inglés
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- Máster
Associate Director Senior Study Lead - Single Sponsor Dedicated (home-based)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Grado
- Teletrabajo opcional
R&D Engineer
Ormco —Madrid, Madrid provincia
- Doctorado
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Director, Site Start up
Precision Medicine Group —Madrid, Madrid provincia
- Teletrabajo
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
3d
National Sales Manager - Medical
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Microsoft Office
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Data Architect
Roche —Madrid, Madrid provincia
- Jornada completa
- Azure
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Site Specialist II
ICON Plc —Madrid, Madrid provincia
- Jornada completa
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1d
Medical Information Specialist with Dutch, French and English
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Grado
- Habilidades organizativas
- Teletrabajo opcional
RWD Analytics Engineer
Roche —Madrid, Madrid provincia
- Jornada completa
- Informática
- Inglés
- Máster
Director, Site Start up
Precision for Medicine —Madrid, Madrid provincia
- Teletrabajo
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Solicitud rápida
3d
Principal Statistical Programmer - FSP (Permanent Homebased) m/w/d
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Informática
- Grado
- Teletrabajo opcional
Sales Development Account Manager - Europe - Remote
Worldwide Clinical Trials —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
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9d
Associate Marketing Director
Veracyte —Madrid, Madrid provincia
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Global Trial Delivery Lead - Sponsor Dedicated
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Máster
- Teletrabajo opcional

Quiero recibir la alerta de empleo más reciente de clinical research en tres cantos, md

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Director, Medical Safety

IQVIA -
Madrid, Madrid provincia

Solicitar ahora

Detalles del empleo

Jornada completa

Beneficios

Teletrabajo opcional

Cualificaciones

Investigación clínica
Investigación
Liderazgo

Descripción completa del empleo

Madrid, Spain | Full time | Home-based | R1558654

Responsibilities

Conduct medical review of clinical trial and post-marketing safety data, including adverse events (AEs), adverse drug reactions (ADRs), coding, causality, expectedness, seriousness assessments, and benefit-risk evaluations.
Provide medical oversight and review of safety documentation, including narratives, aggregate reports, annual and periodic safety reports, risk management plans, regulatory submissions, labeling, protocols, investigator brochures, and case report forms.
Support safety governance activities, including Data Safety Monitoring Boards, Safety Monitoring Committees, medical information escalations, pharmacovigilance oversight, and 24-hour medical support as required.
Serve as Global Safety Physician, project lead, or medical safety advisor, ensuring quality, compliance, operational delivery, training, stakeholder communication, and timely completion of deliverables.
Present safety findings and provide expert medical consultation to clients, internal teams, and cross-functional stakeholders.
Lead and develop medical safety teams through people management, workload planning, performance management, mentoring, training, resource allocation, and succession planning.
Oversee financial, operational, and quality performance of assigned projects, ensuring appropriate resourcing and regulatory compliance.
Contribute to business development activities, including proposals, budgeting, bid defenses, client presentations, strategic planning, and service-line growth initiatives.
Represent the Medical Safety function internally and externally, maintaining key stakeholder relationships and supporting organizational objectives.
Drive continuous improvement through awareness of industry, regulatory, and pharmacovigilance developments, and undertake special projects as required.
Provide global medical safety and pharmacovigilance oversight across clinical development and post-marketing programs.
Lead medical review of safety data, regulatory reports, risk management strategies, and benefit-risk assessments.
Manage medical safety projects, ensuring quality, compliance, stakeholder engagement, and on-time delivery.
Lead, develop, and resource teams of physicians and medical safety professionals globally.
Support business growth through client engagement, proposals, strategic initiatives, and service-line leadership.

Required Knowledge, Skills & Experience

Strong knowledge of global pharmacovigilance, clinical research, safety reporting, Good Clinical Practice (GCP), and applicable regulatory requirements.
In-depth understanding of clinical development, pharmaceutical research, and medical safety/monitoring activities.
Proven ability to manage multiple priorities, meet deadlines, and deliver high-quality outcomes in a complex environment.
Strong consulting, communication, stakeholder management, and relationship-building skills, with the ability to influence clients and cross-functional teams.
Demonstrated leadership capability, including people management, project oversight, financial accountability, and strategic decision-making.
Medical degree (MD or equivalent) from an accredited institution, with substantial clinical practice experience and/or pharmaceutical physician experience.
Significant experience in medical safety, pharmacovigilance, or medical monitoring within the pharmaceutical, biotechnology, CRO, or healthcare industry.
Current medical licensure (or equivalent professional registration) in the country of practice.

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 tres cantos, md

Director, Medical Safety

Business Development Representative (2026-026)

Sr. QA Auditor, GCP/Computerized Systems

Global Team Leader - IVDR

Decision Analytics Consultant

International Product Manager | Endodontics

Manager –Global Advisory Services

Associate Director Senior Study Lead - Single Sponsor Dedicated (home-based)

R&D Engineer

Director, Site Start up

National Sales Manager - Medical

Data Architect

Site Specialist II

Medical Information Specialist with Dutch, French and English

RWD Analytics Engineer

Director, Site Start up

Principal Statistical Programmer - FSP (Permanent Homebased) m/w/d

Sales Development Account Manager - Europe - Remote

Associate Marketing Director

Global Trial Delivery Lead - Sponsor Dedicated

Quiero recibir la alerta de empleo más reciente de clinical research en tres cantos, md

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