20 publicaciones de empleo destacadas de clinical trial 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
Clinical Data Management Lead
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Oracle
- Investigación
- Grado
- Teletrabajo opcional
Técnico/a de Calidad- Pharma Logistics
Alcura —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Inglés
Business Developer - Cell and Gene Therapy (CGT)
Alcura —Barcelona, Barcelona provincia
- Jornada completa
- Ventas
- Inglés
- Microsoft Office
13d
Clinical Development Medical Director - Neuromuscular
Novartis —Barcelona, Barcelona provincia
- De 85.100 € a 158.100 € al año
- Jornada completa
- Trabajo híbrido
- Investigación
- Liderazgo
Senior Biostatistics Supervisor Technician
VHIR —Barcelona, Barcelona provincia
- 38.000 € al año
- Jornada completa
- Trabajo híbrido
- Español
- Doctorado
- Hospital
7h
IT System Engineer - Clinical Trials
Boehringer Ingelheim España, S.A. —Sant Cugat del Vallès, Barcelona provincia
- Jornada completa
- Informática
- Inglés
- AWS
- Abono gimnasio
Global Trial Delivery Lead - Sponsor Dedicated
IQVIA —Barcelona, Barcelona provincia
- Jornada completa
- Inglés
- Investigación
- Máster
- Teletrabajo opcional
VHIR-MSCA-PF-2026.007_Postdoctoral Fellowship (Clinical Neuroimmunology)
VHIR —Barcelona, Barcelona provincia
- Microsoft Access
- Doctorado
- Hospital
Sr Project Specialist. Barcelona. Sponsor dedicated. Preferred experience with Compassionate Use programs
Syneos - Clinical and Corporate - Prod —Barcelona, Barcelona provincia
- Jornada completa
9d
Research Nurse (Nephrology and Transplantation Group)
VHIR —Barcelona, Barcelona provincia
- 29.000 € al año
- Jornada completa
- Español
- Enfermería
- Hospital
12d
Associate Director Patient Centricity - Patient Centered Development Enablement
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Project management
- Grado
9d
Business Subject Matter Expert (Pharma – Clinical Trials).
SDG Group —Barcelona, Barcelona provincia
- Trabajo híbrido
- Español
- Desarrollo de negocios
- Oportunidades de crecimiento y desarrollo profesional
Solicitud rápida
Associate Director, Territory Operations Manager - Cell Therapy
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- CRM software
- Español
- Microsoft Excel
7d
CRA I. Valencia. Sponsor dedicated.
Syneos - Clinical and Corporate - Prod —Barcelona, Barcelona provincia
- Jornada completa
- Grado
5h
Associate Director Patient Centricity - R&D External Partnership Enablement
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Project management
- Grado
9d
VHIR-MSCA-PF-2026.004_Postdoctoral Fellowship (Clinical Neuroimmunology)
VHIR —Barcelona, Barcelona provincia
- Doctorado
- Hospital
- Investigación
RESOLUCIONES DE CONVOCATORIAS 2025
IGTP —Badalona, Barcelona provincia
- Jornada completa
- Enfermería
- Doctorado
- Hospital
- Oportunidades de crecimiento y desarrollo profesional
Solicitud rápida
Global Head of Clinical Safety
Galderma —Barcelona, Barcelona provincia
- Jornada completa
- Trabajo híbrido
- Microsoft Excel
- Doctorado
- Marketing
Research Technician (Stroke Research)
VHIR —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Hospital
6d

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

Al iniciar sesión en tu cuenta, aceptas las Condiciones del servicio de SimplyHired, nuestra Política sobre cookies y nuestra Política de privacidad.

Explorar empleos en más ubicaciones

clinical trial jobs near barcelona, ct

Empleos de Business Developer en Barcelona, Barcelona Provincia

Empleos de Research Technician en Barcelona, Barcelona Provincia

Empleos de Delivery Manager en Barcelona, Barcelona Provincia

Empleos de R&D Engineer en Barcelona, Barcelona Provincia

Empleos de Clinical Data Manager en Barcelona, Barcelona Provincia

Empleos de Full Stack Developer en Valencia, Valencia Provincia

Empleos de Business Developer en Sevilla La Nueva, Madrid Provincia

Empleos de Business Developer en Alga, A Coruña Provincia

Empleos de Business Controller en Madrid Provincia

Empleos de Business Developer en 48314 Isla, Vizcaya Provincia

Empleos de Business Developer en Canovelles, Barcelona Provincia

Empleos de Business Controller en En Remoto

Empleos de Lead Ai Engineer A en Madrid, Madrid Provincia

Empleos de Postdoctoral en 08253 Sant Salvador De Guardiola, Barcelona Provincia

Empleos de Project Engineer en Sant Boi De Llobregat, Barcelona Provincia

Empleos de Learning Development Specialist en Barcelona, Barcelona Provincia

Empleos de Freelance Project Manager en Barcelona, Barcelona Provincia

Empleos de Project Finance en Madrid Provincia

Empleos de Director, Marketing en Donostia San Sebastián, Guipúzcoa Provincia

Empleos de Director Supply Chain en Barcelona, Barcelona Provincia

Risk Surveillance Lead

Novartis -
Barcelona, Barcelona provincia

Solicitar ahora

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 trial empleos en barcelona, ct

Risk Surveillance Lead

Clinical Data Management Lead

Técnico/a de Calidad- Pharma Logistics

Business Developer - Cell and Gene Therapy (CGT)

Clinical Development Medical Director - Neuromuscular

Senior Biostatistics Supervisor Technician

IT System Engineer - Clinical Trials

Global Trial Delivery Lead - Sponsor Dedicated

VHIR-MSCA-PF-2026.007_Postdoctoral Fellowship (Clinical Neuroimmunology)

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

Research Nurse (Nephrology and Transplantation Group)

Associate Director Patient Centricity - Patient Centered Development Enablement

Business Subject Matter Expert (Pharma – Clinical Trials).

Associate Director, Territory Operations Manager - Cell Therapy

CRA I. Valencia. Sponsor dedicated.

Associate Director Patient Centricity - R&D External Partnership Enablement

VHIR-MSCA-PF-2026.004_Postdoctoral Fellowship (Clinical Neuroimmunology)

RESOLUCIONES DE CONVOCATORIAS 2025

Global Head of Clinical Safety

Research Technician (Stroke Research)

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

Related Searches

Explorar empleos en más ubicaciones

Summary

About the Role

Herramientas para candidatos

Herramientas para empresas

Buscar

Mantener la conexión