20 publicaciones de empleo destacadas de clinical research en san sebastián de los reyes, md (¡Están contratando!)

Medical Monitor (Gastroenterology)
PSI CRO —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Investigación
- Microsoft Office
Solicitud rápida
14d
Translation Project Manager – Linguistic Validation and eCOA
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Grado
- Teletrabajo opcional
Medical Engagement Partner Cardiometabolic Diseases - Madrid, CLM y Comunidad Valenciana
Roche —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Máster
Business Development Manager – Medical Affairs Solutions (IQVIA Pharma Review)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Desarrollo de negocios
Associate Principal - Global Custom Integrated Research
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Investigación
- Desarrollo de negocios
Senior Medical Writer - Early Phase (Single Sponsor Support)
Syneos - Clinical and Corporate - Prod —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
14d
Project Manager
NAMSA AKRN Scientific Consulting S.L. —San Sebastián de los Reyes, Madrid provincia
- Jornada completa
- Máster
- Project management
- Grado
Solicitud rápida
4d
Regulatory & Quality Lead – AI IVD Diagnostics
SpotLab —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Español
- Inglés
- Bachillerato
Solicitud rápida
Delegado Derma y Estética - Madrid
IQVIA —Madrid, Madrid provincia
- 30.000 € al año
- Jornada completa
- Habilidades de comunicación
- Enfermería
Associate Medical Director- Neurology
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Desarrollo de negocios
- Teletrabajo opcional
Associate Director, Field Medical Execution - Neuroscience
Novartis —Madrid, Madrid provincia
- De 73.100 € a 135.700 € al año
- Jornada completa
- CRM software
- Doctorado
- Inglés
Associate Pharmacovigilance Project Manager (Europe)
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Project management
- Liderazgo
Solicitud rápida
Medical Safety Director, Clinical Scientist
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Doctorado
- Teletrabajo opcional
1d
CRA I-II in Madrid. Sponsor dedicated.
サイネオス・ヘルス —Madrid, Madrid provincia
- Grado
8d
Senior Director, Drug Development
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Excel
- Investigación
- Teletrabajo opcional
Associate Medical Director, Cardiology , with Metabolic Diseases and Nephrology Experience
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Desarrollo de negocios
- Teletrabajo opcional
Senior Site Contract Associate - IQVIA Biotech
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Investigación
- Microsoft Office
- Grado
- Teletrabajo opcional
Compliance - Senior Consultant (Life Science exp mandatory)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Máster
- Grado
Sr Medical Project Manager
Gilead Sciences —Madrid, Madrid provincia
- Jornada completa
- Español
- Doctorado
- Inglés
8d
Senior Statistician
PSI CRO —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Máster
Solicitud rápida
7d

Quiero recibir la alerta de empleo más reciente de clinical research en san sebastián de los reyes, md

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Medical Monitor (Gastroenterology)

PSI CRO -
Madrid, Madrid provincia

Solicitud rápida

Detalles del empleo

Jornada completa
Hace 14 días

Cualificaciones

Inglés
Investigación
Microsoft Office

Descripción completa del empleo

Company Description

PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights our commitment to delivering high-quality, timely services across a broad spectrum of therapeutic indications.

At PSI, we foster an environment where a diverse range of colleagues feel welcomed and valued. Our inclusive culture is a cornerstone of our success, enabling us to attract and retain top talent globally.

We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry.

Job Description

As part of PSI's Medical Monitoring team, you will join our international group of medical professionals, build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them.

Full-time employment

Hybrid in Madrid or Barcelona, or remote elsewhere in Spain

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and well-being.

Responsibilities:

Serve as medical point of contact for internal project team, study sites and study sponsor for medical matters related to the conduct of clinical trials per protocol and per GCP guidelines
Advise clients, project teams, sites, regulatory agencies and third-party vendors on medical matters
Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, patient narratives, and scientific presentations
Review and analyze of clinical data to ensure the safety of study participants
Ensure that the reported trial data is accurate, complete, and verifiable, and that the conduct of the trial is in compliance with the currently approved protocol/amendments
Address safety issues across the trial from sites and the study team
Provide support for medical data review
Participate in bid defense meetings and proposal activities
Assist in Pharmacovigilance activities
Identify trial risks, and create and implement mitigation strategies with other relevant departments
Organize and lead clinical development advisory boards and safety monitoring boards
Ensure Study team compliance with FDA, EMEA, ICH and GCP guidelines

Qualifications

Medical Doctor degree
Gastroenterology Fellowship certification is a must
Prior experience as a practicing MD (minimum of 10 years)
Prior research and/or clinical trial industry experience is a plus
Full working proficiency in English
Proficiency with MS Office applications
Communication, presentation and analytical skills
Able to work in teams, problem-solving, and detail-oriented

Additional Information

Solicitud rápida

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clinical research empleos en san sebastián de los reyes, md

Medical Monitor (Gastroenterology)

Translation Project Manager – Linguistic Validation and eCOA

Medical Engagement Partner Cardiometabolic Diseases - Madrid, CLM y Comunidad Valenciana

Business Development Manager – Medical Affairs Solutions (IQVIA Pharma Review)

Associate Principal - Global Custom Integrated Research

Senior Medical Writer - Early Phase (Single Sponsor Support)

Project Manager

Regulatory & Quality Lead – AI IVD Diagnostics

Delegado Derma y Estética - Madrid

Associate Medical Director- Neurology

Associate Director, Field Medical Execution - Neuroscience

Associate Pharmacovigilance Project Manager (Europe)

Medical Safety Director, Clinical Scientist

CRA I-II in Madrid. Sponsor dedicated.

Senior Director, Drug Development

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

Senior Site Contract Associate - IQVIA Biotech

Compliance - Senior Consultant (Life Science exp mandatory)

Sr Medical Project Manager

Senior Statistician

Quiero recibir la alerta de empleo más reciente de clinical research en san sebastián de los reyes, md

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