20 publicaciones de empleo destacadas de clinical research en comunidad de madrid (¡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
Clinical Biospecimen Scientist - Single Sponsor Dedicated
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Grado
- Teletrabajo opcional
PV Officer (experience in Medical devices required)
PrimeVigilance —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Inglés
- Gestión del tiempo
Solicitud rápida
11d
Clinical Project Management Director – Patient-Centered Solutions (Multiple Locations)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Investigación
- Desarrollo de negocios
- Liderazgo
Principal, Regulatory Science and Strategy - Real World Solutions
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Doctorado
- Inglés
- Máster
- Teletrabajo opcional
22h
Sr Director, Drug Development Lead
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Excel
- Doctorado
- Teletrabajo opcional
3d
Senior Field Clinical Research Engineer
Boston Scientific —Madrid, Madrid provincia
- Máster
- Grado
2d
Patient & Site Engagement Operations Manager - Sponsor Dedicated (m/w/d)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Word
- Microsoft Excel
- Inglés
- Teletrabajo opcional
Regulatory Affairs Manager
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Office
- Máster
- Grado
- Teletrabajo opcional
6d
Product Data Officer (Medical Devices) - Hybrid / Temporary Contract
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Grado
8d
Associate Safety Project Manager
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Ventas
- Investigación
- Project management
- Teletrabajo opcional
7d
Senior Concierge Corporate Travel Associate
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Microsoft Powerpoint
- Microsoft Word
- Español
Japanese Language Consultant
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Grado
7d
Principal Statistician
PSI CRO —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Máster
Solicitud rápida
Associate Director Senior Study Lead - Single Sponsor Dedicated (home-based)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Grado
- Teletrabajo opcional
Director, PI Market Access, Europe
BD —San Agustín de Guadalix, Madrid provincia
- De 110.400 € a 176.625 € al año
- Español
Medical Information Specialist with Dutch, French and English
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Grado
- Habilidades organizativas
- Teletrabajo opcional
R&D Engineer
Ormco —Madrid, Madrid provincia
- Doctorado
- Informática
- Inglés
- Seguro dental
- Vacaciones pagadas

Quiero recibir la alerta de empleo más reciente de clinical research en comunidad de madrid

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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 comunidad de madrid

Clinical Research Associate

Clinical Business Operations Associate - Portfolio & Operations Support

Associate Clinical Trials Regulatory Manager, EMEA

Clinical Biospecimen Scientist - Single Sponsor Dedicated

PV Officer (experience in Medical devices required)

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

Principal, Regulatory Science and Strategy - Real World Solutions

Sr Director, Drug Development Lead

Senior Field Clinical Research Engineer

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

Regulatory Affairs Manager

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

Associate Safety Project Manager

Senior Concierge Corporate Travel Associate

Japanese Language Consultant

Principal Statistician

Associate Director Senior Study Lead - Single Sponsor Dedicated (home-based)

Director, PI Market Access, Europe

Medical Information Specialist with Dutch, French and English

R&D Engineer

Quiero recibir la alerta de empleo más reciente de clinical research en comunidad de madrid

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