20 publicaciones de empleo destacadas de clinical trials en madrid, md (¡Están contratando!)

Clinical Associate
ICON Plc —Madrid, Madrid provincia
- Jornada completa
- Investigación
- Grado
- Gestión del tiempo
- Seguro dental
- Seguro oftalmológico
4d
Clinical Research Associate 2 - Multi-Sponsor - Based in Barcelona
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Español
- Inglés
- Microsoft Office
- Teletrabajo opcional
Clinical Research Associate 2 - CFSP
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Español
- Inglés
- Microsoft Office
- Teletrabajo opcional
Senior Medical Writer - Early Phase (Single Sponsor Support)
Syneos - Clinical and Corporate - Prod —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
5d
Senior Clinical Research Associate - MedTech
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Field Clinical Research Associate - French Speaking
North American Science Associates Ltd. —San Sebastián de los Reyes, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Máster
Solicitud rápida
22h
Clinical Budget Specialist - FSP Team
Fortrea —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Investigación
- Microsoft Office
- Máster
Clinical Team Lead (CTL)
Evestia Clinical —Madrid, Madrid provincia
- Trabajo híbrido
- Servicio al cliente
- Inglés
- Investigación
Solicitud rápida
11d
Clinical Biospecimen Scientist - Single Sponsor Dedicated
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Grado
- Teletrabajo opcional
Medical Advisor - Temporal - Nutrition (Madrid)
Abbott Laboratories —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Habilidades organizativas
Clinical Trials Vendor Management Specialist
PSI CRO —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Microsoft Office
- Desarrollo de negocios
Solicitud rápida
Clinical Research Lead
Eli Lilly —Alcobendas, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Grado
Study Start Up Associate II
ICON Plc —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Seguro dental
- Seguro oftalmológico
1d
Project Manager II (Clinical)
Evestia Clinical —Madrid, Madrid provincia
- Trabajo híbrido
- Inglés
- Investigación
- Project management
Solicitud rápida
12d
Associate Principal/Principal Qualitative Research, Patient Centered Solutions
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Teletrabajo
- Doctorado
- Inglés
- Investigación
Clinical Trial Assistant Senior
Sermes CRO —Madrid, Madrid provincia
- Inglés
Medical Engagement Partner Cardiometabolic Diseases - Madrid, CLM y Comunidad Valenciana
Roche —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Máster
6d
Medical Engagement Partner Cardiometabolic Diseases - Andalucia, Extremadura, Murcia y Canarias
Roche —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Investigación
- Máster
6d
Medical Advisor Oncology
OncologyPipeline —Madrid, Madrid provincia
- Media jornada
Clinical Trial Manager - IQVIA Biotech
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Investigación
- Project management
- Grado
- Teletrabajo opcional

Quiero recibir la alerta de empleo más reciente de clinical trials en madrid, md

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Clinical Associate

ICON Plc -
Madrid, Madrid provincia

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Detalles del empleo

Jornada completa
Hace 4 días

Beneficios

Seguro dental
Seguro oftalmológico
Plan de pensiones

Cualificaciones

Investigación clínica
Investigación
Grado
Gestión del tiempo

Descripción completa del empleo

Clinical Trial Assistant

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

As a Clinical Associate at ICON, you will support the design, implementation, and management of clinical trials, contributing to the advancement of innovative treatments and therapies.

What You Will Do:

You will contribute to clinical coordination activities, taking responsibility for your deliverables and working collaboratively.

Key responsibilities include:

Assist in the planning, execution, and monitoring of clinical trials, ensuring adherence to protocol requirements, regulatory guidelines, and industry standards.
Coordinate study activities including site initiation, patient recruitment, data collection, and monitoring visits to ensure timely and accurate data collection and documentation.
Collaborate with cross-functional teams including Clinical Operations, Data Management, and Biometrics to support the successful execution of clinical trials.
Maintain comprehensive study documentation and records, ensuring compliance with applicable regulations and standard operating procedures.
Support study close-out activities including data cleaning, analysis, and preparation of clinical study reports.

Your Profile:

You will bring relevant clinical coordination experience, along with the following qualifications and skills.

Required qualifications and experience:

Bachelor's degree in a relevant scientific discipline or healthcare-related field
Previous experience in clinical research or healthcare, preferably within the pharmaceutical, biotechnology, or CRO industry.
Strong organizational and time management skills, with the ability to prioritize tasks and manage competing priorities effectively.
Excellent attention to detail and problem-solving abilities, with a commitment to ensuring data accuracy, integrity, and compliance.
Effective communication and interpersonal skills, with the ability to collaborate cross-functionally and build strong relationships with study teams and clinical sites.
Willingness to travel as required (approximately 60%)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request .

Are you a current ICON Employee?

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Refina tu búsqueda

clinical trials empleos en madrid, md

Clinical Associate

Clinical Research Associate 2 - Multi-Sponsor - Based in Barcelona

Clinical Research Associate 2 - CFSP

Senior Medical Writer - Early Phase (Single Sponsor Support)

Senior Clinical Research Associate - MedTech

Field Clinical Research Associate - French Speaking

Clinical Budget Specialist - FSP Team

Clinical Team Lead (CTL)

Clinical Biospecimen Scientist - Single Sponsor Dedicated

Medical Advisor - Temporal - Nutrition (Madrid)

Clinical Trials Vendor Management Specialist

Clinical Research Lead

Study Start Up Associate II

Project Manager II (Clinical)

Associate Principal/Principal Qualitative Research, Patient Centered Solutions

Clinical Trial Assistant Senior

Medical Engagement Partner Cardiometabolic Diseases - Madrid, CLM y Comunidad Valenciana

Medical Engagement Partner Cardiometabolic Diseases - Andalucia, Extremadura, Murcia y Canarias

Medical Advisor Oncology

Clinical Trial Manager - IQVIA Biotech

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