20 publicaciones de empleo destacadas de clinical project en madrid, md (¡Están contratando!)

Clinical Trial Safety Scientist (FSP - Permanent Home Based)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Doctorado
- Gestión del tiempo
- Teletrabajo opcional
Clinical Trial Manager - IQVIA Biotech
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Investigación
- Project management
- Grado
- Teletrabajo opcional
Senior Site Contract Associate - IQVIA Biotech
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Investigación
- Microsoft Office
- Grado
- Teletrabajo opcional
Associate Principal / Principal, Clinical Outcome Assessment (COA) Strategy Consulting
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Doctorado
- Investigación
- Máster
Compliance - Senior Consultant (Life Science exp mandatory)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Máster
- Grado
Clinical Trials Vendor Management Specialist
PSI CRO —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Microsoft Office
- Desarrollo de negocios
Solicitud rápida
Medical Scientist Lead
Gilead Sciences —Madrid, Madrid provincia
- Jornada completa
- Español
- Doctorado
- Inglés
Global Trial Delivery Lead - Sponsor Dedicated
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Máster
- Teletrabajo opcional
Legal Counsel EMEA M&A
IQVIA —Madrid, Madrid provincia
- De 180.300 € a 383.100 € al año
- Jornada completa
- Trabajo híbrido
- Inglés
- Grado
Training & Education Specialist, Urology - EMEA (Sacral Neuromodulation)
Boston Scientific —Madrid, Madrid provincia
- Trabajo híbrido
- Inglés
- Project management
- Marketing
Provider Relations Analyst Europe | German Speaker
The Cigna Group —Pozuelo de Alarcón, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Excel
- Inglés
Patient Safety & Medical Affairs Delivery Manager
Roche —Madrid, Madrid provincia
- Jornada completa
- Agile
- Liderazgo
- Negociación
Diagnostic Liason - Galicia y Castilla y León
AstraZeneca —Madrid, Madrid provincia
- Jornada completa
- Microsoft Excel
- Doctorado
- Ventas
8d
Business Account Specialist - Cantabria, País Vasco, Palencia y León
AstraZeneca —Madrid, Madrid provincia
- Jornada completa
- Microsoft Excel
- Inglés
- Grado
Iberian Country Marketer (m/f/x)*
Solventum —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Español
- Microsoft Excel
12d
Decision Analytics Consultant
Roche —Madrid, Madrid provincia
- Jornada completa
- Español
- Microsoft Excel
- Informática
Associate Principal - Global Custom Integrated Research
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Investigación
- Desarrollo de negocios
Senior Director, Drug Development
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Excel
- Investigación
- Teletrabajo opcional
Business Area Manager - Breast Cancer
AstraZeneca —Madrid, Madrid provincia
- Jornada completa
- Microsoft Excel
- Grado
- Liderazgo
Business Account Specialist - Andalucía
AstraZeneca —Madrid, Madrid provincia
- Jornada completa
- Microsoft Excel
- Ventas
- Inglés
5d

Quiero recibir la alerta de empleo más reciente de clinical project en madrid, md

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Clinical Trial Safety Scientist (FSP - Permanent Home Based)

IQVIA -
Madrid, Madrid provincia

Solicitar ahora

Detalles del empleo

Jornada completa

Beneficios

Teletrabajo opcional

Cualificaciones

Doctorado
Gestión del tiempo

Descripción completa del empleo

Madrid, Spain | Full time | Home-based | R1521994

Responsibilities

Ensure consistent processes and efficient review of critical clinical/safety data
Review of patient-level clinical/safety data on an ongoing basis to ensure medical accuracy and completeness, coding consistency and generate applicable queries as needed to obtain information for appropriate medical assessment and case closure
Prepare aggregated data visualization and facilitate meetings related to review of safety data on study level
Contribute to study start-up activities according to the applicable process/procedures (ex. input to the applicable documents, tools set up)
Serve as a member of the Extended Study Team and report on TRISARC deliverables
Work with the study physicians and/or clinical/project scientists to support standardized high-level data review and medical evaluation
Escalate urgent and critical medical cases to the study physician/medical scientist as appropriate
Provide input into the process of setting automated patient narratives, if applicable
Provide input to establishing the process for handwritten patient narratives, including guideline development and the quality control process if applicable
Lead quality of own deliverables
Take on tasks as assigned by the Directors, Associate Directors Clinical Trial Safety
Provide input into non-drug project work including training activities, continuous improvement and development of procedures as needed

Education/Experience

Educational degree (BSc/Msc/PhD) in Life Science or equivalent work experience in directly related fields

Minimum 2+ years of experience in Pharmacovigilance / Drug Safety
Understanding of the clinical study and drug development process
Knowledge of ICH/GCP Guidelines
Knowledge of SAE reporting requirements

Experience using data review tools is preferred
Quality focus, analytical skills, and ability to concisely summarize large amounts of complex information
Proven ability to prioritize and manage multiple tasks with conflicting deadlines
Excellent time management
Very good interpersonal and communication skills
Team player, able to work individually
Ability and willingness to work cross-functionally, e.g. with internal and external partners, on global studies, across different phases of drug development or different therapy areas

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.

At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

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 project empleos en madrid, md

Clinical Trial Safety Scientist (FSP - Permanent Home Based)

Clinical Trial Manager - IQVIA Biotech

Senior Site Contract Associate - IQVIA Biotech

Associate Principal / Principal, Clinical Outcome Assessment (COA) Strategy Consulting

Compliance - Senior Consultant (Life Science exp mandatory)

Clinical Trials Vendor Management Specialist

Medical Scientist Lead

Global Trial Delivery Lead - Sponsor Dedicated

Legal Counsel EMEA M&A

Training & Education Specialist, Urology - EMEA (Sacral Neuromodulation)

Provider Relations Analyst Europe | German Speaker

Patient Safety & Medical Affairs Delivery Manager

Diagnostic Liason - Galicia y Castilla y León

Business Account Specialist - Cantabria, País Vasco, Palencia y León

Iberian Country Marketer (m/f/x)*

Decision Analytics Consultant

Associate Principal - Global Custom Integrated Research

Senior Director, Drug Development

Business Area Manager - Breast Cancer

Business Account Specialist - Andalucía

Quiero recibir la alerta de empleo más reciente de clinical project en madrid, md

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