Clinical Research Associate - Sponsor dedicated Spain

IQVIA; España; Presencial; EUR 30.000 - 40.000; Jornada completa

Descripción de la vacante

A leading clinical research organization in Spain seeks a talented Junior CRA to join their dedicated team. This role entails performing site-related tasks, supporting subject recruitment, and ensuring compliance with regulatory standards. Ideal candidates will have a university degree in a scientific discipline and experience in the Pharma industry. Proficiency in both Spanish and English is essential. This position promises an excellent working environment within a reputable organization, with opportunities for career growth and an attractive benefits package.

Servicios

Mobile phone

Attractive benefits package

Support for flexible work schedules

Resources for career growth

Formación

• University degree in scientific discipline or health care.
• Experience in Pharma Industry or Clinical Trials.
• Very good computer skills including MS Office.
• Excellent command of Spanish and English language.
• Organizational, time management and problem-solving skills required.
• Ability to establish effective working relationships.
• Flexibility to travel.
• Driver’s license class B.

Responsabilidades

• Perform site selection, initiation, monitoring, and close-out visits.
• Support development of a subject recruitment plan.
• Evaluate quality of site practices according to regulatory requirements.
• Track regulatory submissions and data query resolutions.
• Collaborate with experts at study sites and client representatives.

Conocimientos

Organizational skills

Time management

Problem-solving skills

Excellent command of Spanish

Excellent command of English

Educación

University degree in scientific discipline or health care

Herramientas

MS Office

Descripción del empleo

Overview

IQVIA Spain is looking for talented and motivated team member 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:

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

Qualifications:

• University degree in scientific discipline or health care
• Experience in Pharma Industry, and/or Clinical Trials environment
• Very good computer skills including MS Office
• Excellent command of Spanish and English language
• Organizational, time management and problem-solving skills
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients
• Flexibility to travel
• Driver’s license class B

What you can expect:

• Resources that promote your career growth
• Leaders that support flexible work schedules
• Programs to help you build your therapeutic knowledge
• Excellent working environment in a stabile, international, reputable company
• Mobile phone and attractive benefits package