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 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 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
Principal, Regulatory Science and Strategy - Real World Solutions
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Doctorado
- Inglés
- Máster
- Teletrabajo opcional
20h
Patient & Site Engagement Operations Manager - Sponsor Dedicated (m/w/d)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Word
- Microsoft Excel
- Inglés
- Teletrabajo opcional
Product Data Officer (Medical Devices) - Hybrid / Temporary Contract
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Grado
8d
International Product Manager | Endodontics
Henry Schein España S.L. —Madrid, Madrid provincia
- 41.000 € al año
- Jornada completa
- Trabajo híbrido
- Español
- Marketing
- Inglés
Associate Safety Project Manager
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Ventas
- Investigación
- Project management
- Teletrabajo opcional
7d
Global Trial Delivery Lead - Sponsor Dedicated
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Máster
- Teletrabajo opcional
Senior Field Clinical Research Engineer
Boston Scientific —Madrid, Madrid provincia
- Máster
- Grado
2d
Senior Concierge Corporate Travel Associate
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Microsoft Powerpoint
- Microsoft Word
- Español
Regulatory Affairs Manager
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Office
- Máster
- Grado
- Teletrabajo opcional
6d
Decision Analytics Consultant
Roche —Madrid, Madrid provincia
- Jornada completa
- Español
- Microsoft Excel
- Informática
Associate Director Senior Study Lead - Single Sponsor Dedicated (home-based)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Grado
- Teletrabajo opcional
Medical Information Specialist with Dutch, French and English
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Grado
- Habilidades organizativas
- Teletrabajo opcional
Associate Marketing Director
Veracyte —Madrid, Madrid provincia
- Teletrabajo
- Marketing
- Liderazgo
- Marketing
Solicitud rápida
R&D Engineer
Ormco —Madrid, Madrid provincia
- Doctorado
- Informática
- Inglés
- Seguro dental
- Vacaciones pagadas

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Clinical Research Associate

Opis s.r.l.
Madrid, Madrid provincia

Solicitar ahora

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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Refina tu búsqueda

clinical research empleos en alcobendas, md

Clinical Research Associate

Clinical Business Operations Associate - Portfolio & Operations Support

Associate Clinical Trials Regulatory Manager, EMEA

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

PV Officer (experience in Medical devices required)

Clinical Biospecimen Scientist - Single Sponsor Dedicated

Principal, Regulatory Science and Strategy - Real World Solutions

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

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

International Product Manager | Endodontics

Associate Safety Project Manager

Global Trial Delivery Lead - Sponsor Dedicated

Senior Field Clinical Research Engineer

Senior Concierge Corporate Travel Associate

Regulatory Affairs Manager

Decision Analytics Consultant

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

Medical Information Specialist with Dutch, French and English

Associate Marketing Director

R&D Engineer

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

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