20 publicaciones de empleo destacadas de clinical associate en spain (¡Están contratando!)

Clinical Scientist Associate Director
Amgen —En remoto
- Teletrabajo
- Doctorado
- Máster
- Grado
2h
Consultant - Clinical Operations (Remote - Europe)
Veeva Systems —En remoto
- Jornada completa
- Teletrabajo
- Español
- Informática
- Ventas
- Teletrabajo opcional
Senior CRA
ICON Plc —Madrid, Madrid provincia
- Jornada completa
- Investigación
- Grado
- Abono gimnasio
Fraud Analyst – Payment Integrity
The Cigna Group —Pozuelo de Alarcón, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Inglés
- Microsoft Office
- Seguro dental
International Regulatory Capability and Process Excellence Associate Director
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Inglés
- Investigación
14d
Senior Project Coordinator, EU
Indero —En remoto
- Teletrabajo
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Solicitud rápida
Python Engineer - OpenData Clinical
Veeva Systems —En remoto
- Jornada completa
- Teletrabajo
- Inglés
- Oficina
- AWS
- Teletrabajo opcional
- Abono gimnasio
Associate Director Study Start Up
TFS HealthScience —Barcelona, Barcelona provincia
- Enfermería
- Servicio al cliente
- Investigación
Solicitud rápida
Set Up Designer
Ormco —Madrid, Madrid provincia
- Español
- Inglés
- Bachillerato
Senior Site Contracts Associate, IQVIA Biotech
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Word
- Microsoft Excel
- Habilidades de presentación
Account Manager Surgery Madrid & Castilla La Mancha
BD —San Agustín de Guadalix, Madrid provincia
- Español
- Ventas
- Hospital
Analyst, PAE
Alira Health —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Senior Clinical Data Manager
TFS HealthScience —Sevilla, Sevilla provincia
- Teletrabajo
- Informática
- Grado
Solicitud rápida
9d
Principal Biostatistician (Biomarker Analyst -EMEA and US BASED)
サイネオス・ヘルス —Madrid, Madrid provincia
- Inglés
COA (Clinical Outcome Assessment) Lead
ICON Plc —Madrid, Madrid provincia
- Jornada completa
- Doctorado
- Máster
- Habilidades de análisis
- Seguro dental
- Seguro oftalmológico
Associate Marketing Manager (Professional Education)
Dexcom —En remoto
- Jornada completa
- Teletrabajo
- Marketing
- Inglés
- Grado
Study Project Manager I
AbbVie —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Investigación
- Oficina
- Grado
12d
CTM/Sr CTM - EMEA - FSP
Thermo Fisher Scientific —En remoto
- Jornada completa
- Teletrabajo
- Inglés
- Máster
- Grado
8h
Associate Director, Medical Affairs
Vertex Pharmaceuticals —Madrid, Madrid provincia
- Jornada completa
- Doctorado
- Investigación
- Administración y dirección de empresas
Director, Global Medical Training
Alexion Pharmaceuticals,Inc. —Barcelona, Barcelona provincia
- Doctorado
- Investigación
- Seguro oftalmológico
2d

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Clinical Scientist Associate Director

Amgen -
En remoto

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Detalles del empleo

Hace 2 horas

Cualificaciones

Doctorado
Máster
Grado
Liderazgo

Descripción completa del empleo

Spain - Remote

JOB ID: R-246860 LOCATION: Spain - Remote WORK LOCATION TYPE: Flex Commuter / Hybrid DATE POSTED: Jun. 03, 2026 CATEGORY: Clinical SALARY RANGE: 90,787.65 EUR - 122,830.35 EUR

What you will do

In this role, the Clinical Scientist Associate Director supports the design, execution, and oversight of clinical trials and other late-phase global clinical studies. The role contributes to protocol development, study execution, medical monitoring support, and clinical data review, ensuring delivery of high-quality, decision-ready clinical data for regulatory submissions and scientific dissemination.

Support the design, start-up, and execution of global clinical trials, ensuring adherence to protocol, regulatory requirements, and data integrity standards.
Contribute to development of clinical protocols, statistical analysis plans, investigator brochures, and regulatory documents, with focus on study endpoints, key efficacy outcomes, and safety assessments.
Collaborate with cross-functional teams to support endpoint strategy, event adjudication processes, and safety monitoring.
Participate in development and oversight of endpoint adjudication charters, safety monitoring plans, and Data Monitoring Committee (DMC) interactions.
Provide clinical input into data management plans, CRF design, and clinical data review, with focus on key study endpoints, efficacy and safety outcomes, and/or imaging or biomarker endpoints, as applicable.
Conduct ongoing clinical data review and signal detection, supporting identification and resolution of safety and data quality issues across global trial sites.
Support preparation and interpretation of interim analyses, database lock activities, and top-line data readouts.
Assist Development Lead and Clinical Scientist Director with medical monitoring activities and oversight of CROs, vendors, and adjudication committees.
Collaborate with clinical operations, biostatistics, safety, regulatory, and medical affairs teams to ensure successful delivery of clinical studies across relevant indications and endpoint strategies.
Contribute to clinical study reports, regulatory submissions, scientific publications, and presentations for internal and external stakeholders.
Identify operational or scientific risks and proactively implement mitigation strategies across cross-functional teams.

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is a leader with these qualifications.

Basic Qualifications:

Doctorate degree and 3 years of life sciences/healthcare experience

Master’s degree and 5 years of life sciences/healthcare experience

Bachelor’s degree and 7 years of life sciences/healthcare experience

Preferred Qualifications:

3 years of pharmaceutical clinical drug development experience, including experience supporting late-stage, global clinical trials.
Demonstrated experience contributing to clinical trial process improvements within a therapeutic area or study team environment
Industry or academic experience in a relevant therapeutic area and/or clinical trials; experience in large global studies preferred.
Strong communication and presentation skills, with the ability to clearly convey scientific concepts and clinical data to cross-functional teams and leadership audiences, both written and oral
Experience supporting the design, monitoring, and implementation of clinical trials in compliance with Good Clinical Practice standards and applicable regulatory requirements
Working knowledge of study data readout activities, including data cleaning, database lock, data extraction, endpoint validation, and generation of analysis outputs to support topline and final results.
Experience contributing to regulatory submission documents and supporting clinical regulatory responses for health authority interactions under guidance
Experience serving as a contributing author on scientific publications or data presentations for internal forums or scientific conferences
Experience in clinical data review and analysis tools such as Spotfire, listings review platforms, or other data visualization and analysis tools.

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clinical associate empleos en spain

Clinical Scientist Associate Director

Consultant - Clinical Operations (Remote - Europe)

Senior CRA

Fraud Analyst – Payment Integrity

International Regulatory Capability and Process Excellence Associate Director

Senior Project Coordinator, EU

Python Engineer - OpenData Clinical

Associate Director Study Start Up

Set Up Designer

Senior Site Contracts Associate, IQVIA Biotech

Account Manager Surgery Madrid & Castilla La Mancha

Analyst, PAE

Senior Clinical Data Manager

Principal Biostatistician (Biomarker Analyst -EMEA and US BASED)

COA (Clinical Outcome Assessment) Lead

Associate Marketing Manager (Professional Education)

Study Project Manager I

CTM/Sr CTM - EMEA - FSP

Associate Director, Medical Affairs

Director, Global Medical Training

Quiero recibir la alerta de empleo más reciente de clinical associate en spain

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