20 publicaciones de empleo destacadas de clinical research en tres cantos, 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
Clinical Project Management Director – Patient-Centered Solutions (Multiple Locations)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Investigación
- Desarrollo de negocios
- Liderazgo
Clinical Biospecimen Scientist - Single Sponsor Dedicated
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Grado
- Teletrabajo opcional
Patient & Site Engagement Operations Manager - Sponsor Dedicated (m/w/d)
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Word
- Microsoft Excel
- Inglés
- Teletrabajo opcional
Principal, Regulatory Science and Strategy - Real World Solutions
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Doctorado
- Inglés
- Máster
- Teletrabajo opcional
23h
Product Data Officer (Medical Devices) - Hybrid / Temporary Contract
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Grado
8d
Senior Field Clinical Research Engineer
Boston Scientific —Madrid, Madrid provincia
- Máster
- Grado
2d
Global Trial Delivery Lead - Sponsor Dedicated
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Máster
- Teletrabajo opcional
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
Regulatory Affairs Manager
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Office
- Máster
- Grado
- Teletrabajo opcional
6d
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
Japanese Language Consultant
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Grado
7d
Sales Development Account Manager - Europe - Remote
Worldwide Clinical Trials —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- CRM software
- Ventas
- Salesforce
EMEA Marketing Director
Insightec —Madrid, Madrid provincia
- Jornada completa
- Ventas
- Sistemas ERP
- Inglés
Solicitud rápida
National Sales Manager - Medical
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Microsoft Office
- Grado
Principal Statistical Programmer - FSP (Permanent Homebased) m/w/d
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Informática
- Grado
- Teletrabajo opcional

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

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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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Refina tu búsqueda

clinical research empleos en tres cantos, 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)

Clinical Biospecimen Scientist - Single Sponsor Dedicated

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

Principal, Regulatory Science and Strategy - Real World Solutions

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

Senior Field Clinical Research Engineer

Global Trial Delivery Lead - Sponsor Dedicated

Associate Safety Project Manager

Senior Concierge Corporate Travel Associate

Regulatory Affairs Manager

Medical Information Specialist with Dutch, French and English

Associate Marketing Director

Japanese Language Consultant

Sales Development Account Manager - Europe - Remote

EMEA Marketing Director

National Sales Manager - Medical

Principal Statistical Programmer - FSP (Permanent Homebased) m/w/d

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

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