Clinical Research Associate- Sponsor Dedicated

TN Spain; Madrid; Presencial; EUR 30.000 - 50.000; Jornada completa

Descripción de la vacante

Una empresa internacional y reputada busca un Asociado de Investigación Clínica para unirse a su equipo en Madrid. Este rol ofrece la oportunidad de trabajar en diversas áreas terapéuticas y desarrollar una carrera significativa. Las responsabilidades incluyen la selección y monitoreo de sitios de investigación, así como la gestión de relaciones con expertos y clientes. Con un entorno de trabajo excelente y recursos que promueven el crecimiento profesional, esta posición es ideal para quienes buscan un impacto en la ciencia de la salud. Si tienes pasión por la investigación clínica y deseas contribuir a un mundo más saludable, esta es la oportunidad perfecta para ti.

Servicios

Coche de empresa

Teléfono móvil

Paquete de beneficios atractivo

Horarios de trabajo flexibles

Recursos para el crecimiento profesional

Formación

• Grado universitario en disciplina científica o atención médica.
• Experiencia en la industria farmacéutica o ensayos clínicos.

Responsabilidades

• Realizar visitas de selección, inicio, monitoreo y cierre de sitios.
• Colaborar con expertos en sitios de estudio y representantes del cliente.

Conocimientos

Organizational Skills

Time Management

Problem-Solving Skills

Bilingual (Spanish and English)

Interpersonal Skills

Flexibility to Travel

Educación

University Degree in Scientific Discipline

Experience in Pharma Industry

Experience in Clinical Trials Environment

Herramientas

Mobile Phone

Company Car

Descripción del empleo

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Clinical Research Associate- Sponsor Dedicated, Madrid

Client: IQVIA

Location: Madrid, Spain

Job Category: Other

EU work permit required: Yes

Job Views: 2

Posted: 25.04.2025

Expiry Date: 09.06.2025

Job Description:

Clinical Research Associate

IQVIA Spain is looking for talented and motivated team members to join our Sponsor dedicated team as junior CRA. At this position, you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas and build a meaningful, strong career within our organization.

Your responsibilities will include:

1. Performing site selection, initiation, monitoring, and close-out visits
2. Supporting the development of a subject recruitment plan
3. Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines
4. Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions
5. Collaborating with experts at study sites and with client representatives

Qualifications:

1. University degree in a scientific discipline or health care
2. Experience in Pharma Industry, and/or Clinical Trials environment
3. Excellent command of Spanish and English language
4. Organizational, time management, and problem-solving skills
5. Ability to establish and maintain effective working relationships with coworkers, managers, and clients
6. Flexibility to travel
7. Driver’s license class B

What you can expect:

1. Resources that promote your career growth
2. Leaders that support flexible work schedules
3. Programs to help you build your therapeutic knowledge
4. Excellent working environment in a stable, international, reputable company
5. Company car, mobile phone, and attractive benefits package

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at