20 publicaciones de empleo destacadas de clinical research en alcobendas, md (¡Están contratando!)

Clinical Research Associate
Opis s.r.l. —Madrid, Madrid provincia
- Hasta 48.000 € al año
- Jornada completa
- Inglés
- Microsoft Office
8d
Clinical Trial Site Relationship Coordinator
Medpace, Inc. —Madrid, Madrid provincia
- Jornada completa
- Español
- Inglés
- Investigación
Associate Clinical Trials Regulatory Manager, EMEA
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Investigación
- Desarrollo de negocios
- Project management
- Teletrabajo opcional
Clinical Business Operations Associate - Portfolio & Operations Support
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Excel
- Investigación
- Teletrabajo opcional
Global Team Leader - IVDR
SGS —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Inglés
- Investigación
- Oficina
Solicitud rápida
Artificial Intelligence Research Scientist
SpotLab —Madrid, Madrid provincia
- Jornada completa
- Español
- Doctorado
- Informática
Solicitud rápida
Product Data Officer (Medical Devices) - Hybrid / Temporary Contract
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Grado
8d
Delegad@ Hospitalario - Madrid
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Habilidades organizativas
- Habilidades de comunicación
- Formación continua
Site Enrollment and Engagement Lead
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Grado
- Teletrabajo opcional
PV Officer (experience in Medical devices required)
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Inglés
- Gestión del tiempo
Solicitud rápida
11d
Associate Safety Project Manager
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Ventas
- Investigación
- Project management
- Teletrabajo opcional
7d
Clinical Project Management Director – Patient-Centered Solutions (Multiple Locations)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Investigación
- Desarrollo de negocios
- Liderazgo
Regulatory Affairs Manager
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Office
- Máster
- Grado
- Teletrabajo opcional
6d
Manager, COA Service Offerings & Quality
IQVIA —Madrid, Madrid provincia
- Horas extra
- Inglés
- Investigación
- Microsoft Office
- Teletrabajo opcional
7d
Nutriasesor Hospital y Residencias - Madrid
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Hospital
- Habilidades de comunicación
- Formación continua
- Ayuda al desarrollo profesional
22h
Principal, Regulatory Science and Strategy - Real World Solutions
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Doctorado
- Inglés
- Máster
- Teletrabajo opcional
22h
Senior/ Medical Writer - FSP (M/W/D)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Microsoft Word
- Doctorado
- Investigación
Senior Site Contract Associate - IQVIA Biotech
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Investigación
- Microsoft Office
- Grado
- Teletrabajo opcional
Core Information Offering Specialist - MedTech
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Excel
- Inglés
- Teletrabajo opcional
Sr Medical Project Manager
Gilead Sciences —Madrid, Madrid provincia
- Jornada completa
- Español
- Doctorado
- Inglés

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Clinical Research Associate

Opis s.r.l.
Madrid, Madrid provincia

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Detalles del empleo

Jornada completa
Hasta 48.000 € al año
Hace 8 días

Cualificaciones

Inglés
Microsoft Office

Descripción completa del empleo

The Clinical Research Associate is responsible for managing and monitoring clinical trials to ensure they are conducted in compliance with study protocols, ICH-GCP, and applicable regulations. This includes site selection, initiation, monitoring, and close-out activities, while ensuring data quality and patient safety. The role reports to the Clinical Project Manager.

Key Responsibilities

Identify, assess, and initiate investigational sites
Conduct feasibility, pre-study, initiation, monitoring, and close-out visits
Ensure compliance with protocols, SOPs, ICH-GCP, and regulatory requirements
Perform source data verification and ensure data accuracy and completeness
Monitor patient recruitment and support sites in meeting targets
Ensure proper reporting of adverse events and protocol deviations
Manage investigational product handling, storage, and accountability
Maintain study documentation (TMF/eTMF, Investigator Files)
Write monitoring reports and follow-up communications
Collaborate with project teams, sponsors, and site staff
Support audits/inspections and mentor junior CRAs

Requirements

Degree in a scientific field
Minimum 2 years’ CRA or clinical trial monitoring experience (oncology and phase 1 studies highly desirable)
Strong knowledge of ICH-GCP, ISO14155, and clinical trial processes
Good English and Microsoft Office skills
Strong organizational, communication, and problem-solving abilities
Ability to work independently and in a team

What we offer

Salary up to EUR 48,000/annually based on experience
Additional benefits
Opportunity to develop your career with and expanding company

Please read the information notice on the processing of personal data in the candidates information section of our company website.

Who we are

Founded in 1998 in Italy and now operating at an international level, OPIS is a full-service science driven biotech focused CRO providing premium trial management for multi-country clinical trials, including state-of-the-art information technology solutions and innovative approaches to the increasing complexity and variety of current projects.

OPIS added value lies in its highly specialized professionals who can assist their clients using their deep know-how and experience to guarantee a top-quality level of Clinical Trial Management and ability to operate in a wide range of fields (medical writing, scientific and statistical consultancy for trial design, regulatory activities, pharmacovigilance, etc.) always contributing to our clients’ challenging achievements.

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clinical research empleos en alcobendas, md

Clinical Research Associate

Clinical Trial Site Relationship Coordinator

Associate Clinical Trials Regulatory Manager, EMEA

Clinical Business Operations Associate - Portfolio & Operations Support

Global Team Leader - IVDR

Artificial Intelligence Research Scientist

Product Data Officer (Medical Devices) - Hybrid / Temporary Contract

Delegad@ Hospitalario - Madrid

Site Enrollment and Engagement Lead

PV Officer (experience in Medical devices required)

Associate Safety Project Manager

Clinical Project Management Director – Patient-Centered Solutions (Multiple Locations)

Regulatory Affairs Manager

Manager, COA Service Offerings & Quality

Nutriasesor Hospital y Residencias - Madrid

Principal, Regulatory Science and Strategy - Real World Solutions

Senior/ Medical Writer - FSP (M/W/D)

Senior Site Contract Associate - IQVIA Biotech

Core Information Offering Specialist - MedTech

Sr Medical Project Manager

Quiero recibir la alerta de empleo más reciente de clinical research en alcobendas, md

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