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

GLOBAL MEDICAL OPERATIONS MANAGER
Almirall —Barcelona, Barcelona provincia
- Jornada completa
- Inglés
- Máster
- Grado
VHIR-MSCA-PF-2026.009_Postdoctoral Fellowship (Biomedical Gynaecology)
VHIR —Barcelona, Barcelona provincia
- Doctorado
- Hospital
- Inglés
Study Director Team Lead
Novartis —Barcelona, Barcelona provincia
- De 74.200 € a 137.800 € al año
- Jornada completa
- Investigación
- Project management
- Grado
22h
Contract Analyst I
ICON Plc —Barcelona, Barcelona provincia
- Jornada completa
- Investigación
- Negociación
- Seguro dental
- Seguro oftalmológico
1d
Senior Project Manager / Associate Project Management Director
Optimapharm d.o.o. —Barcelona, Barcelona provincia
- De 80.000 € a 100.000 € al año
- Jornada completa
- Teletrabajo
- Inglés
- Investigación
- Máster
5d
Sr Project Specialist. Barcelona. Sponsor dedicated. Preferred experience with Compassionate Use programs
サイネオス・ヘルス —Barcelona, Barcelona provincia
9d
HTA & Modelling Science Lead
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Oficina
- Grado
Solution Lead - Study Design Platform
Merck KGaA —Mollet del Vallès, Barcelona provincia
- Informática
- Inglés
- Máster
Lead Data Scientist - BCN/MAD/Munich
ailylabs —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Oficina
- SQL
- Machine learning
Solicitud rápida
RESOLUCIONES DE CONVOCATORIAS 2026
IGTP —Badalona, Barcelona provincia
- Jornada completa
- Enfermería
- Doctorado
- Hospital
- Seguro oftalmológico
- Oportunidades de crecimiento y desarrollo profesional
Solicitud rápida
Biostatistician
Sanofi —Barcelona, Barcelona provincia
- De 48.000 € a 64.000 € al año
- Doctorado
- Inglés
- Máster
Associate Medical Director- Neurology
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Inglés
- Desarrollo de negocios
- Teletrabajo opcional
Global Head, RWE Biostatistics
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Investigación
- Máster
- Grado
- Teletrabajo opcional
1d
Precision Medicine Director
Novartis —Barcelona, Barcelona provincia
- De 85.100 € a 158.100 € al año
- Jornada completa
- Trabajo híbrido
- Investigación
- Liderazgo
- Plan de pensiones
VHIR-MSCA-PF-2026.016_Postdoctoral Fellowship (Infection and Immunity in Paediatric Patients)
VHIR —Barcelona, Barcelona provincia
- Doctorado
- Hospital
- Inglés
Medical Strategy Lead, Oncology (Home-Based)
IQVIA —Barcelona, Barcelona provincia
- Horas extra
- Inglés
- Investigación
- Desarrollo de negocios
- Teletrabajo opcional
Physiotherapist (Physical medicine and rehabilitation)
VHIR —Barcelona, Barcelona provincia
- Media jornada
- Español
- Hospital
- Inglés
7d
Project Specialist in Public Procurement, Tender Management & Trade Effectiveness - VIE Contract
Sanofi —Barcelona, Barcelona provincia
- Microsoft Powerpoint
- Microsoft Excel
- Inglés
21h
Sales Manager (Medical Device)
Neuroelectrics —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Ventas
- Inglés
- Seguro dental
QA SENIOR MANAGER
Almirall —Sant Feliu de Llobregat, Barcelona provincia
- Jornada completa
- Inglés

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GLOBAL MEDICAL OPERATIONS MANAGER

Almirall -
Barcelona, Barcelona provincia

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Detalles del empleo

Jornada completa

Cualificaciones

Biología
Inglés
Máster
Grado
Farmacia

Descripción completa del empleo

We’re building the future of medical dermatology by focusing on unmet patient needs and giving people the space to think independently, take ownership and make an impact that matters.

Our purpose is simple: to transform patients’ lives by addressing real needs. We work with care, act with courage, keep things simple and focus our innovation where it makes a difference.

Recognised as a Top Employer in Spain since 2008 and in Germany since 2025, we continue to invest in an environment where people can grow and move forward.

If you care differently, you belong here.

Mission

The Global Medical Operations Manager is responsible for the operational planning, coordination, and oversight of Global Medical Affairs studies, with a strong focus on Investigator-Initiated Studies (IIS), Phase IV / non-interventional studies, and Real-World Evidence (RWE) initiatives.

The role ensures end-to-end operational excellence, compliance, transparency, and cross-functional alignment across global and local teams, enabling timely evidence generation to support Global Medical strategy.

Key Responsibilities

1. Investigator-Initiated Studies (IIS) & Global Medical Grants Management

Act as the global operational owner for IIS and selected global medical grants:

Serve as primary operational point of contact for globally supported IIS
Coordinate IIS activities across Legal, Compliance, Finance, Clinical Trial Supply, R&D, IP, CROs, global and local teams
Lead and coordinate:
- Contract generation and execution with HCPs/HCOs
- Amendment management in collaboration with Legal and affiliates
- Budget monitoring and reporting
Maintain global IIS master documentation, including:
- Proposals and approvals
- Agreements and amendments
- Invoice tracking and payment documentation
- Final report/publication tracking (links or references, as applicable)
Track study progress, milestones, and deliverables in collaboration with affiliates
Manage the full invoice and payment lifecycle, ensuring timely and accurate processing
Ensure transparency reporting for global IIS and grants in applicable systems (e.g. Veeva), in line with local legislation (with particular attention to high-complexity markets such as France and the US)
Provide quarterly IIS KPI reporting in line with Global Medical Affairs guidance
Support pharmacovigilance requirements by ensuring IIS operational data is available for PSUR, DSUR, and PSMF activities (upon request and per SOP)

2. Global Phase IV, RWE, and Non-Interventional Studies

Provide operational experience and support for Global Medical evidence generation initiatives, including RWE:

Support the planning, execution, and oversight of company-sponsored Phase IV, low-interventional, and non-interventional studies
Act as the main operational contact for CROs, ensuring quality, timelines, and budget adherence
Support Global Medical Leads in delivering evidence aligned with Brand Plans and Medical Strategy
Track and maintain an overview of globally sponsored and locally executed GMA studies, ensuring visibility, consistency, and governance
Maintain accurate and timely study updates to support:
- Pharmacovigilance reporting
- Public registry disclosure obligations
- Internal governance and decision-making forums

3. Cross-Functional Governance & Stakeholder Engagement

Actively participate in Phase IV / IIS Review Committee when IIS proposals are presented and discussed
Coordinate follow-up actions after IIS approval and ensure alignment across stakeholders
Collaborate closely with:
- Global and Local Medical Affairs teams
- Finance (budget tracking and long-term projections)
- Global Compliance and QA
- Legal (for contracts)
- CRO partners and external vendors
Contribute to medical operations updates, including internal communication updates, enabling informed decisions within Global Medical Affairs
Attend selected scientific meetings, operational forums, and internal trainings as relevant to role scope

4. Process Optimization, SOP Ownership & Digital Innovation

Lead the review, update, and implementation of key Medical Operations SOPs related to studies
Maintain and update the Medical Operations Hub and study-specific operational pages, ensuring accuracy, relevance, and alignment with Global Medical needs
Proactively identify opportunities for digital solutions and emerging technologies (e.g., workflow automation, analytics, AI-assisted processes) to improve efficiency and data quality in studies management

Education

University degree in Pharmacy, Biology, Chemistry, Life Sciences , or equivalent

Experience

Proven experience in:
- Clinical operations, medical operations, or study management
- Phase IV, non-interventional, or RWE studies
- Cross-functional coordination in a global matrix environment
Solid understanding of:
- Transparency and compliance requirements
- Study governance and lifecycle management
Experience in Dermatology or related therapeutic areas is an asset
Fluent in English (written and spoken)

Competencies & Values

Operational Excellence: Structured, detail-oriented, and delivery-focused
Collaboration: Able to work effectively across functions, cultures, and geographies
Ownership & Accountability: Takes responsibility for global activities and outcomes
Innovation & Simplicity: Seeks practical solutions and continuous improvement
Patient-Centric Mindset: Keeps scientific integrity and patient impact at the core

Our Values

Care – We listen, empathize, and support each other
Courage – We challenge the status quo and take ownership
Innovation – We create meaningful, patient-centered solutions
Simplicity – We act decisively and keep things clear and effective

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clinical trial empleos en barcelona, ct

GLOBAL MEDICAL OPERATIONS MANAGER

VHIR-MSCA-PF-2026.009_Postdoctoral Fellowship (Biomedical Gynaecology)

Study Director Team Lead

Contract Analyst I

Senior Project Manager / Associate Project Management Director

Sr Project Specialist. Barcelona. Sponsor dedicated. Preferred experience with Compassionate Use programs

HTA & Modelling Science Lead

Solution Lead - Study Design Platform

Lead Data Scientist - BCN/MAD/Munich

RESOLUCIONES DE CONVOCATORIAS 2026

Biostatistician

Associate Medical Director- Neurology

Global Head, RWE Biostatistics

Precision Medicine Director

VHIR-MSCA-PF-2026.016_Postdoctoral Fellowship (Infection and Immunity in Paediatric Patients)

Medical Strategy Lead, Oncology (Home-Based)

Physiotherapist (Physical medicine and rehabilitation)

Project Specialist in Public Procurement, Tender Management & Trade Effectiveness - VIE Contract

Sales Manager (Medical Device)

QA SENIOR MANAGER

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