20 publicaciones de empleo destacadas en assist in clinical trials (¡Están contratando!)

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Clinical trial associate
ICON Plc —Barcelona, Barcelona provincia
- Jornada completa
- Investigación
- Grado
- Seguro dental
- Seguro oftalmológico
1d
Assistant CRA
Thermo Fisher Scientific —Barcelona, Barcelona provincia
- Jornada completa
- Servicio al cliente
- Inglés
- Microsoft Office
Clinical Trial Coordinator
Thermo Fisher Scientific —Madrid, Madrid provincia
- Jornada completa
- Español
- Inglés
- Grado
CRA II, Multisponsor ** Hybrid MADRID or BARCELONA **
Syneos - Clinical and Corporate - Prod —Barcelona, Barcelona provincia
- Jornada completa
- Grado
1d
Junior Project Coordinator in the Central Lab department
Anapharm Bioanalytics —Barcelona, Barcelona provincia
- Microsoft Word
- Microsoft Excel
- Inglés
11d
Senior Clinical Trial Assistant
Pivotal —Madrid, Madrid provincia
- Inglés
- Experiencia administrativa
- Bachillerato
CRA II, Multisponsor ** Hybrid MADRID or BARCELONA **
サイネオス・ヘルス —Barcelona, Barcelona provincia
- Grado
1d
CRA I, Multisponsor ** Hybrid MADRID or BARCELONA **
サイネオス・ヘルス —Barcelona, Barcelona provincia
- Grado
1d
Clinical Trial Assistant (Diabetes and Metabolism Research Group)
VHIR —Barcelona, Barcelona provincia
4d
Consultant - Clinical Operations (Remote - Europe)
Veeva Systems —En remoto
- Jornada completa
- Teletrabajo
- Español
- Informática
- Ventas
- Teletrabajo opcional
Site Activation Specialist II. Location in Madrid. FSP. Hybrid model.
サイネオス・ヘルス —Madrid, Madrid provincia
- Trabajo híbrido
- Hospital
- Grado
11d
CRA I, Multisponsor ** Hybrid MADRID or BARCELONA **
Syneos - Clinical and Corporate - Prod —Madrid, Madrid provincia
- Jornada completa
- Grado
1d
Senior Project Coordinator, EU
Indero —En remoto
- Teletrabajo
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Solicitud rápida
Senior Site Contract Associate - IQVIA Biotech
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Investigación
- Microsoft Office
- Grado
Site Contract Specialist II in Barcelona. Sponsor dedicated.
サイネオス・ヘルス —Barcelona, Barcelona provincia
Single Sponsor Senior Medical Editor - Must have previous clinical editing exp.
サイネオス・ヘルス —Barcelona, Barcelona provincia
Clinical Researcher (Neurodegenerative Diseases Research Group)
VHIR —Barcelona, Barcelona provincia
- Jornada completa
- Español
- Hospital
- Inglés
5d
Principal Biostatistician (Biomarker Analyst -EMEA and US BASED)
サイネオス・ヘルス —Madrid, Madrid provincia
- Inglés
Director, Medical Affairs (m/f/d)
Abbott Laboratories —Madrid, Madrid provincia
Clinical Scientist Associate Director
Amgen —En remoto
- Teletrabajo
- Doctorado
- Máster
- Grado
6d

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Clinical trial associate

ICON Plc -
Barcelona, Barcelona provincia

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Detalles del empleo

Jornada completa
Hace 1 día

Beneficios

Seguro dental
Seguro oftalmológico
Plan de pensiones

Cualificaciones

Investigación clínica
Investigación
Grado

Descripción completa del empleo

Clinical Trial Associate

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 Trial Associate at ICON, you will assist with the design and analysis of clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.

Key responsibilities include:

Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
Support the preparation of study-related materials, such as informed consent forms and case report forms.
Work with cross-functional teams to facilitate communication and ensure smooth trial execution.
Contribute to the tracking and reporting of clinical trial metrics and milestones.

Your Profile:

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

Required qualifications and experience:

Bachelor's degree in a scientific or healthcare-related field.
Prior experience or strong interest in clinical research.
Knowledge of clinical trial processes, regulations, and guidelines.
Excellent organizational and communication skills.
Ability to work collaboratively in a fast-paced environment with attention to detail.
Willingness to travel as required (approximately 10%)

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 here.

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assist in clinical trials empleos

Clinical trial associate

Assistant CRA

Clinical Trial Coordinator

CRA II, Multisponsor Hybrid MADRID or BARCELONA

Junior Project Coordinator in the Central Lab department

Senior Clinical Trial Assistant

CRA II, Multisponsor Hybrid MADRID or BARCELONA

CRA I, Multisponsor Hybrid MADRID or BARCELONA

Clinical Trial Assistant (Diabetes and Metabolism Research Group)

Consultant - Clinical Operations (Remote - Europe)

Site Activation Specialist II. Location in Madrid. FSP. Hybrid model.

CRA I, Multisponsor Hybrid MADRID or BARCELONA

Senior Project Coordinator, EU

Senior Site Contract Associate - IQVIA Biotech

Site Contract Specialist II in Barcelona. Sponsor dedicated.

Single Sponsor Senior Medical Editor - Must have previous clinical editing exp.

Clinical Researcher (Neurodegenerative Diseases Research Group)

Principal Biostatistician (Biomarker Analyst -EMEA and US BASED)

Director, Medical Affairs (m/f/d)

Clinical Scientist Associate Director

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