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
9d
Clinical Business Operations Associate - Portfolio & Operations Support
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Excel
- Investigación
- Teletrabajo opcional
Associate Clinical Trials Regulatory Manager, EMEA
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Investigación
- Desarrollo de negocios
- Project management
- Teletrabajo opcional
Research Nurse - Madrid
IQVIA —Madrid, Madrid provincia
- Media jornada
- Microsoft Word
- Microsoft Excel
- Microsoft Access
9d
Clinical Project Management Director – Patient-Centered Solutions (Multiple Locations)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Investigación
- Desarrollo de negocios
- Liderazgo
PV Officer (experience in Medical devices required)
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Inglés
- Gestión del tiempo
Solicitud rápida
11d
Clinical Biospecimen Scientist - Single Sponsor Dedicated
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Grado
- Teletrabajo opcional
Delegad@ Hospitalario - Madrid
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Habilidades organizativas
- Habilidades de comunicación
- Formación continua
Global Team Leader - IVDR
SGS —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Inglés
- Investigación
- Oficina
Solicitud rápida
Senior/ Medical Writer - FSP (M/W/D)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Microsoft Word
- Doctorado
- Investigación
Site Enrollment and Engagement Lead
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Grado
- Teletrabajo opcional
Central Monitoring Manager
PSI CRO —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Español
- Microsoft Excel
- Inglés
Solicitud rápida
Sr Director, Drug Development Lead
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Excel
- Doctorado
- Teletrabajo opcional
3d
Consultant – Global Advisory Services
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Máster
- Project management
Safety Associate Medical Information Coordinator with Greek and French, German or Italian
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Microsoft Office
- Grado
- Teletrabajo opcional
7d
Principal, Regulatory Science and Strategy - Real World Solutions
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Doctorado
- Inglés
- Máster
- Teletrabajo opcional
23h
Patient & Site Engagement Operations Manager - Sponsor Dedicated (m/w/d)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Word
- Microsoft Excel
- Inglés
- Teletrabajo opcional
HR Coordinator
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Español
- Microsoft Office
- Grado
10d
Product Data Officer (Medical Devices) - Hybrid / Temporary Contract
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Grado
8d
Associate Director, Public Affairs, Europe
Ascendis Pharma —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Doctorado
- Inglés
- Oficina
Solicitud rápida

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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 9 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 Business Operations Associate - Portfolio & Operations Support

Associate Clinical Trials Regulatory Manager, EMEA

Research Nurse - Madrid

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

PV Officer (experience in Medical devices required)

Clinical Biospecimen Scientist - Single Sponsor Dedicated

Delegad@ Hospitalario - Madrid

Global Team Leader - IVDR

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

Site Enrollment and Engagement Lead

Central Monitoring Manager

Sr Director, Drug Development Lead

Consultant – Global Advisory Services

Safety Associate Medical Information Coordinator with Greek and French, German or Italian

Principal, Regulatory Science and Strategy - Real World Solutions

Patient & Site Engagement Operations Manager - Sponsor Dedicated (m/w/d)

HR Coordinator

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

Associate Director, Public Affairs, Europe

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

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