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

Risk Surveillance Lead
Novartis —Barcelona, Barcelona provincia
- De 63.600 € a 118.000 € al año
- Jornada completa
- Inglés
- Oficina
- Grado
Postdoctoral Fellow (Ref. PD/26/11)
IRB Barcelona —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Doctorado
- Inglés
9d
Analyst, PAE
Alira Health —Barcelona, Barcelona provincia
- De 20.000 € a 22.000 € al año
- Jornada completa
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Study Director Team Lead
Novartis —Barcelona, Barcelona provincia
- De 74.200 € a 137.800 € al año
- Jornada completa
- Investigación
- Project management
- Grado
8d
Medical Safety Lead - CRM
Novartis —Barcelona, Barcelona provincia
- De 69.000 € a 128.100 € al año
- Jornada completa
- Enfermería
- Inglés
- Inteligencia artificial
20h
Principal, Health Economics, Health Technology Assessment
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Microsoft Excel
- Máster
- Inteligencia artificial
Global Program Safety Lead - CRM
Novartis —Barcelona, Barcelona provincia
- De 85.100 € a 158.100 € al año
- Jornada completa
- CRM software
- Doctorado
- Inglés
20h
SSU CRA II Barcelona. Sponsor dedicated
サイネオス・ヘルス —Barcelona, Barcelona provincia
- Grado
6d
Associate Medical Director- Neurology
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Inglés
- Desarrollo de negocios
- Teletrabajo opcional
Project Manager
Barcelona Institute for Global Health (ISGlobal) —Barcelona, Barcelona provincia
- Media jornada
- Español
- Doctorado
- Inglés
9d
Amics del VHIR - Institutional call for the incorporation of Early-stage (R1) researchers
VHIR —Barcelona, Barcelona provincia
- De 19.563 € a 25.079 € al año
- Microsoft Excel
- Doctorado
- Hospital
6d
MEDICAL AFFAIRS SENIOR MANAGER
Almirall —Barcelona, Barcelona provincia
- Jornada completa
- Doctorado
- Inglés
- Investigación
Associate Medical Director, Cardiology , with Metabolic Diseases and Nephrology Experience
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Inglés
- Desarrollo de negocios
- Teletrabajo opcional
RESOLUCIONES DE CONVOCATORIAS 2025
IGTP —Badalona, Barcelona provincia
- Jornada completa
- Enfermería
- Doctorado
- Hospital
- Oportunidades de crecimiento y desarrollo profesional
Solicitud rápida
Data Science Consultant, Discovery & Translational Science
Clarivate —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Doctorado
- Inglés
Senior Director, Drug Development
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Excel
- Investigación
- Teletrabajo opcional
Senior Statistician
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Doctorado
- Inglés
Scientific Computing Officer — HPC Systems & Performance (ref. AD/26/09)
IRB Barcelona —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Inglés
- C++
Senior Demand Planning, Staff Analyst
Beckman Coulter Diagnostics —Barcelona, Barcelona provincia
- Jornada completa
- Inglés
- Oficina
- Máster
- Vacaciones pagadas
Associate Manager – Global Pricing (HTA and Pricing Reporting)
Sanofi —Barcelona, Barcelona provincia
- De 48.000 € a 64.000 € al año
- Jornada completa
- Microsoft Powerpoint
- Microsoft Excel
- Inglés

Quiero recibir la alerta de empleo más reciente de clinical research en barcelona, ct

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Risk Surveillance Lead

Novartis -
Barcelona, Barcelona provincia

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Detalles del empleo

Jornada completa
De 63.600 € a 118.000 € al año

Cualificaciones

Inglés
Grado
Optimización de la conversión

Descripción completa del empleo

Summary

The Risk-Based Quality Management (RBQM) Risk surveillance Lead is responsible driving the adoption of RBQM practice at trial level and oversee the implementation, and continuous improvement. Risk Surveillance Lead works within a matrix environment and has overall account-ability for the surveillance of the quality risks across the assigned trials and program, enabling a comprehensive clinical quality (GCP) risk governance. The role demonstrates leadership in influencing and improving clinical trial quality through the expert understanding of clinical trial protocols, processes, regulatory requirements, and quality management principles.

Please note that Novartis cannot sponsor visas for this location. Relocation is not available.

#LI-Hybrid
On site expectation of 12 days per month/ave. 3 days per week in the office.

About the Role

Major Accountabilities:

Facilitate trial protocol risk assessment across multiple cross-functional domains (clinical, operational, data management, vendors, regulatory etc.) associated to critical-to-quality (CtQ) data and processes, including definition of quality tolerance limits (QTLs), evaluation of risks based on likelihood, detectability, impact, and ensures mitigation strategy / plans are defined
Responsible for drafting, maintaining, and archiving the study specific documentation of risk management activities e.g., Integrated Quality Risk Management Plan (IQRMP)
Partners with the RBQM system configuration team to ensure risk indicators, quality tolerance limits and other analytics/visualizations are programmed and functioning per operational requirements in the RBQM system
Conduct of periodic central surveillance of the aggregate data at the study and potentially program level, leveraging available analytics/visualizations in the RBQM system, to identify emerging risks and/or issues
Facilitate risk review meetings and discussions with study and potentially program team members to effectively communicate and discuss the findings, support, and encourage robust root cause identification and mitigation strategies
Supports and participates in internal and external audits and inspection
Collaborate with training departments to support training initiatives and aid in the adoption of the RBQM approach.
Identifies and shares lessons learned, best practices, successes, case studies, failures, and process improvement opportunities to promote continuous improvement and consistency with RBQM processes
Acts as a change agent, champion, subject matter expert and point of contact of RBQM methodology, leading study teams to understand and follow the best practices to achieve maximum benefit

Experience:

Bachelor’s Degree in a health-related, life science area, or equivalent combination of education, training, and work experience

Minimum of 4 years of experience in the pharmaceutical or CRO industry
Preferred minimum of 1 years of experience in Risk Based Quality Management
Robust understanding of the drug development process and clinical trial execution
Knowledge of industry regulatory standards including 21 CFR Part 11, ICH E6, ICH E8 (GCP)
Experience in risk management, sponsor audits and health authority inspections, root cause analyses and mitigation strategies as well as Corrective Actions Preventive Actions
Knowledge of RBQM IT systems or other data analytic systems
Demonstrated ability to analyze data, identify patterns and make recommendations for improvement
Demonstrated ability to effectively lead cross functional team meetings
Experience forming cross-functional collaborations; strong interpersonal skills
Supports a culture of continual improvement and innovation; promotes knowledge sharing
Ability to influence without authority
Thinks creatively; challenges the status quo

Languages:

English: fluent written and spoken

Benefits & RewardsAt Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen.The expected Annual Base Salary Range for this role: 63,600.00 - 118,000.00 EUR AnnualThe base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically.In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters.The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave.Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics. Read our brochure to learn more about our global total rewards offering: https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process. Commitment to Diversity and Inclusion / EEONovartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve.

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.
Read our handbook (PDF 30 MB)

Primary location salary range

€63,600.00 - €118,000.00

Division

Development

Business Unit

Development

Location

Spain

Site

Barcelona Gran Vía

Company / Legal Entity

ES06 (FCRS = ES006) Novartis Farmacéutica, S.A.

Functional Area

Research & Development

Job Type

Full time

Employment Type

Regular

Shift Work

Solicitar ahora

Refina tu búsqueda

clinical research empleos en barcelona, ct

Risk Surveillance Lead

Postdoctoral Fellow (Ref. PD/26/11)

Analyst, PAE

Study Director Team Lead

Medical Safety Lead - CRM

Principal, Health Economics, Health Technology Assessment

Global Program Safety Lead - CRM

SSU CRA II Barcelona. Sponsor dedicated

Associate Medical Director- Neurology

Project Manager

Amics del VHIR - Institutional call for the incorporation of Early-stage (R1) researchers

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Associate Medical Director, Cardiology , with Metabolic Diseases and Nephrology Experience

RESOLUCIONES DE CONVOCATORIAS 2025

Data Science Consultant, Discovery & Translational Science

Senior Director, Drug Development

Senior Statistician

Scientific Computing Officer — HPC Systems & Performance (ref. AD/26/09)

Senior Demand Planning, Staff Analyst

Associate Manager – Global Pricing (HTA and Pricing Reporting)

Quiero recibir la alerta de empleo más reciente de clinical research en barcelona, ct

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